Quaternary ammonium compounds useful as muscarinic receptor antagonists

ABSTRACT

The invention provides compounds of the formula: 
                         
in salt or zwitterionic form or a pharmaceutically acceptable salt thereof, wherein R 1-6 , a, Z and Q are as defined in the specification. These compounds are muscarinic receptor antagonists. The invention also provides pharmaceutical compositions containing such compounds, processes for preparing such compounds and methods of using such compounds to, for example, treat pulmonary disorders such as chronic obstructive pulmonary disease and asthma.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional application of U.S. Ser. No. 13/921,396, filed Jun. 19, 2013, now allowed; which is a divisional application of U.S. Ser. No. 13/473,792, filed May 17, 2012, now U.S. Pat. No. 8,492,407; which is a divisional application of U.S. Ser. No. 12/148,887, filed Apr. 23, 2008, now U.S. Pat. No. 8,202,891, which claims the benefit of U.S. Provisional Application No. 60/925,951, filed on Apr. 24, 2007; the entire disclosures of which are incorporated herein by reference in their entirety.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to quaternary ammonium compounds having muscarinic receptor antagonist or anticholinergic activity. The invention also relates to pharmaceutical compositions comprising these compounds, processes for preparing them and methods of use to treat pulmonary disorders.

2. State of the Art

Pulmonary or respiratory disorders, such as chronic obstructive pulmonary disease (COPD) and asthma, afflict many millions of people worldwide and such disorders are a leading cause of morbidity and mortality. Muscarinic receptor antagonists are known to provide bronchoprotective effects and therefore, such compounds are useful for treating respiratory disorders, such as COPD and asthma. When used to treat such disorders, muscarinic receptor antagonists are typically administered by inhalation. However, even when administered by inhalation, a significant amount of the muscarinic receptor antagonist is often absorbed into the systemic circulation resulting in systemic side effects, such as dry mouth, mydriasis and cardiovascular side effects. Additionally, many inhaled muscarinic receptor antagonists have a relatively short duration of action requiring that they be administered several times per day. Such a multiple-daily dosing regime is not only inconvenient but also creates a significant risk of inadequate treatment due to patient non-compliance with the required frequent dosing schedule.

Accordingly, a need exists for new muscarinic receptor antagonists. In particular, a need exists for muscarinic receptor antagonists having high potency, reduced systemic side effects when administered by inhalation, and a long duration of action thereby allowing for once-daily or even once-weekly dosing. In addition, a need exists for muscarinic receptor antagonists having high affinity for the receptor and a long receptor half life. Such compounds are expected to be particularly effective for treating pulmonary disorders, such as COPD and asthma, while reducing or eliminating side effects, such as dry-mouth and constipation.

SUMMARY OF THE INVENTION

The present invention provides novel quaternary ammonium compounds which have muscarinic receptor antagonist or anticholinergic activity. Among other properties, compounds of this invention have been found to possess improved binding affinity for hM₂ and hM₃ muscarinic receptor subtypes, have longer receptor half-lives, have a larger therapeutic window, or have greater potency compared to related compounds. Accordingly, compounds of the invention are expected to be useful and advantageous as therapeutic agents for treating pulmonary disorders.

One aspect of the invention relates to compounds having formula I:

in salt or zwitterionic form, wherein:

R¹ is selected from —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl, —C₁₋₃alkylene-SCH₃, —C₃₋₉cycloalkyl, and heteroaryl; R² is an aryl or heteroaryl group; R³ is selected from H and —C₀₋₁alkylene-OH; or when R′ is —C₃₋₉cycloalkyl, R³ can form a double bond with the carbon atom on the —C₃₋₉cycloalkyl group; or —CR¹R² together form a group of formula:

a is 0 or an integer of from 1 to 3; each R⁴ is independently selected from fluoro and —C₁₋₄alkyl;

R⁵ is selected from —C₁₋₅alkyl and —C₀₋₁alkyleneC₃₋₅cycloalkyl;

R⁶ is selected from —C₁₋₃alkyl, —C₁₋₂alkyleneC₃₋₇cycloalkyl, —C₀₋₄alkylene-OH, —C₁₋₂alkylene-C(O)O—C₁₋₄alkyl, and —C₁₋₂alkylene-C(O)NR^(6a)R^(6b); where R^(6a) and R^(6b) are independently selected from H and —C₁₋₄alkyl; or R⁶ is taken with R⁵ to form —C₃₋₅alkylene-;

Z is selected from a bond, —O—, —S—, —S(O)—, —SO₂—, —SO₂—NR^(Z1)—, —NR^(Z1)—SO₂—, —C(O)—, —OC(O)—, —C(O)O—, —NR^(Z1)C(O)—, —C(O)NR^(Z1)—, —NR^(Z2)—C(O)—NR^(Z3)—, —NR^(Z2)—C(S)—NR^(Z3)—, —CH(OH)—, and —C(═N—O—R^(Z4))—; where R^(Z1) is selected from H and —C₁₋₄alkyl; R^(Z2) and R^(Z3) are independently selected from H, —C₁₋₄alkyl, and —C₃₋₆cycloalkyl, or R^(Z2) and R^(Z3) are taken together to form —C₂₋₄alkylene- or —C₂₋₃alkenylene-; and R^(Z4) is selected from —C₁₋₄alkyl and benzyl; and

Q is an aryl or heteroaryl group;

wherein the —C₃₋₉cycloalkyl in R¹ and the aryl in R² are optionally substituted with 1 to 5 R groups independently selected from —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, —C₃₋₆cycloalkyl, cyano, halo, —OR^(a), —SR^(a), —S(O)R^(a), —S(O)₂R^(a), and —NR^(b)R^(c); where each R^(a) is independently selected from H, —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, and —C₃₋₆cycloalkyl; and each R^(b) and R^(c) is independently selected from H, —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, and —C₃₋₆cycloalkyl; wherein the aryl in Q is optionally substituted with 1 to 5 R^(Q) groups independently selected from halo, —C₁₋₄alkyl, —C₀₋₄alkylene-OH, cyano, —C₀₋₂alkylene-COOH, —C(O)O—C₁₋₄alkyl, —S—C₁₋₄alkyl, —NH—C(O)—C₁₋₄alkyl, —N-di-C₁₋₄alkyl, and —N⁺(O)O; wherein each alkyl, alkylene, alkenyl, alkenylene, alkynyl, and cycloalkyl group in R, R³⁻⁶, Z, Q, and R^(Q), is optionally substituted with 1 to 5 fluoro atoms; and each —CH₂— group in —(CH₂)₁₋₄— is optionally substituted with 1 or 2 substituents independently selected from —C₁₋₂alkyl, —OH, fluoro, and phenyl; and pharmaceutically acceptable salts thereof.

Another aspect of the invention relates to quaternary ammonium compounds having formula II:

and pharmaceutically acceptable salts thereof, where X⁻ is an anion of a pharmaceutically acceptable acid; and R¹⁻⁶, a, Z and Q are as defined for formula I.

Among the compounds of formula I, compounds of particular interest are those having an inhibition dissociation constant (K_(i)) for binding to the M₃ receptor subtype of less than or equal to 100 nM; in particular having a K_(i) less than or equal to 50 nM; more particularly having a K_(i) less than or equal to 10 nM; and even more particularly having a K_(i) less than or equal to 1.0 nM.

Another aspect of the invention relates to pharmaceutical compositions comprising a pharmaceutically acceptable carrier and a compound of the invention. Such compositions may optionally contain other therapeutic agents such as steroidal anti-inflammatory agents (e.g., corticosteroids), β₂ adrenergic receptor agonists, phosphodiesterase-4 inhibitors, and combinations thereof. Accordingly, in yet another aspect of the invention, a pharmaceutical composition comprises a compound of the invention, a second active agent, and a pharmaceutically acceptable carrier. Another aspect of the invention pertains to a combination of active agents, comprising a compound of the invention and a second active agent. The compound of the invention can be formulated together or separately from the additional agent(s). When formulated separately, a pharmaceutically acceptable carrier may be included with the additional agent(s). Thus, yet another aspect of the invention relates to a combination of pharmaceutical compositions, the combination comprising: a first pharmaceutical composition comprising a compound of the invention and a first pharmaceutically acceptable carrier; and a second pharmaceutical composition comprising a second active agent and a second pharmaceutically acceptable carrier. This invention also relates to a kit containing such pharmaceutical compositions, for example where the first and second pharmaceutical compositions are separate pharmaceutical compositions.

Compounds of the invention possess muscarinic receptor antagonist activity, and are therefore expected to be useful as therapeutic agents for treating patients suffering from a disease or disorder that is treated by blocking the muscarinic receptor. Thus, one aspect of the invention is directed to a method of producing bronchodilation in a patient, comprising administering to the patient a bronchodilation-producing amount of a compound of the invention. The invention is also directed to method of treating a pulmonary disorder such as chronic obstructive pulmonary disease or asthma, comprising administering to a patient a therapeutically effective amount of a compound of the invention. Another aspect of the invention relates to a method for antagonizing a muscarinic receptor in a mammal comprising administering to the mammal, a muscarinic receptor-antagonizing amount of a compound of the invention.

Since compounds of the invention possess muscarinic receptor antagonist activity, such compounds are also useful as research tools. Accordingly, one aspect of the invention pertains to a method of using a compound of the invention as a research tool, the method comprising conducting a biological assay using a compound of the invention. Compounds of the invention can also be used to evaluate new chemical compounds. Thus another aspect of the invention relates to a method of evaluating a test compound in a biological assay, comprising: (a) conducting a biological assay with a test compound to provide a first assay value; (b) conducting the biological assay with a compound of the invention to provide a second assay value; wherein step (a) is conducted either before, after or concurrently with step (b); and (c) comparing the first assay value from step (a) with the second assay value from step (b). Exemplary biological assays include a muscarinic receptor binding assay and a bronchoprotection assay in a mammal. Still another aspect of the invention is directed to a method of studying a biological system or sample comprising a muscarinic receptor, the method comprising: (a) contacting the biological system or sample with a compound of the invention; and (b) determining the effects caused by the compound on the biological system or sample.

The invention is also directed to processes and intermediates useful for preparing compounds of the invention. Accordingly, another aspect of the invention relates to a process of preparing compounds of the invention, comprising: (a) reacting a compound of formula 1 with a compound of formula 2 or reacting a compound of formula 1′ with a compound of formula 2′ to produce a compound of formula 3, and reacting the compound of formula 3 with an organic substrate containing an R⁶ group; or (b) reacting a compound of formula 4 with a compound of formula 2; or (c) reacting a compound of formula 4 with a compound of formula 5 to produce a compound of formula 6, and reacting the compound of formula 6 with a compound of formula 7; and recovering the product in salt or zwitterionic form, to provide a compound of formula I; wherein compounds of formula 1, 1′, 2, 2′, and 3-7 are as defined herein. In other aspects, the invention is directed to products prepared by any of the processes described herein.

Yet another aspect of the invention is directed to the use of a compound of the invention for the manufacture of a medicament, especially for the manufacture of a medicament useful for treating a pulmonary disorder (such as chronic obstructive pulmonary disease and asthma), for producing bronchodilation, or for antagonizing a muscarinic receptor in a mammal. Still another aspect of the invention pertains to the use of a compound of the invention as a research tool. Other aspects and embodiments of the invention are disclosed herein.

DETAILED DESCRIPTION OF THE INVENTION

The invention is directed to compounds having formula I:

in salt or zwitterionic form, or a pharmaceutically acceptable salt thereof. More specifically, the invention is directed to quaternary ammonium compounds having formula II:

or a pharmaceutically acceptable salt thereof, where X⁻ is an anion of a pharmaceutically acceptable acid. The term “quaternary ammonium compound” refers to a compound that is derived from ammonium hydroxide or from an ammonium salt, wherein all four hydrogen atoms of the NH₄ ⁻ion have been replaced by organic groups.

As used herein, the term “compound of the invention” is intended to include compounds of formula I as well as the species embodied in formulas such as II, IIa, IIb, IIc, IId, IIe, and IIf. The compounds of the invention are quaternary ammonium salts and may be converted between different salt forms using state of the art methodologies, for example, using ion exchange chromatography. Also, the compounds can be obtained in the form of solvates, and such solvates are included within the scope of this invention. Accordingly, those skilled in the art will recognize that reference to a compound herein, for example, reference to a “compound of the invention” includes reference to a compound of formula I as well as to any pharmaceutically acceptable salt forms and pharmaceutically acceptable solvates of that compound unless otherwise indicated.

The compounds of the invention may contain one or more chiral centers and so may exist in a number of stereoisomeric forms. When such chiral centers are present, this invention is directed to racemic mixtures, pure stereoisomers (i.e., enantiomers or diastereomers), stereoisomer-enriched mixtures, and the like unless otherwise indicated. When a chemical structure is depicted without any stereochemistry, it is understood that all possible stereoisomers are encompassed by such structure. Thus, for example, the term “compound of formula I” is intended to include all possible stereoisomers of the compound. Similarly, when a particular stereoisomer is shown or named herein, it will be understood by those skilled in the art that minor amounts of other stereoisomers may be present in the compositions of this invention unless otherwise indicated, provided that the utility of the composition as a whole is not eliminated by the presence of such other isomers. Individual enantiomers may be obtained by numerous methods that are well known in the art, including chiral chromatography using a suitable chiral stationary phase or support, or by chemically converting them into diastereomers, separating the diasteromers by conventional means such as chromatography or recrystallization, then regenerating the original enantiomers. Additionally, where applicable, all cis-trans or E/Z isomers (geometric isomers), tautomeric forms and topoisomeric forms of the compounds of this invention are included within the scope of this invention unless otherwise specified.

In particular, the compounds of formula I contain a chiral center at the carbon atom indicated by the symbol * in the following partial formula (shown without optional substituents for clarity):

In one embodiment of this invention, the carbon atom identified by the symbol * has the (R) configuration. In this embodiment, compounds of formula I have the (R) configuration at the carbon atom identified by the symbol * or are enriched in a stereoisomeric form having the (R) configuration at this carbon atom. In another embodiment, the carbon atom identified by the symbol * has the (S) configuration. In this embodiment, compounds of formula I have the (S) configuration at the carbon atom identified by the symbol * or are enriched in a stereoisomeric form having the (S) configuration at this carbon atom.

The compounds of the invention, as well as those compounds used in their synthesis, may also include isotopically-labeled compounds, i.e., where one or more atoms have been enriched with atoms having an atomic mass different from the atomic mass predominately found in nature. Examples of isotopes that may be incorporated into the compounds of formula I, for example, include, but are not limited to, ²H, ³H, ¹³C, ¹⁴C, ¹⁵N, ¹⁸O and ¹⁷O.

The compounds of the invention have been found to possess muscarinic receptor antagonist activity. Among other properties, compounds of the invention have been found to possess improved binding affinity for hM₂ and hM₃ muscarinic receptor subtypes, have longer receptor half-lives, and have greater potency compared to related compounds, and are expected to be useful as therapeutic agents for treating pulmonary disorders.

The nomenclature used herein to name the compounds of the invention is illustrated in the Examples herein. This nomenclature has been derived using the commercially-available AutoNom software (MDL, San Leandro, Calif.).

Representative Embodiments

The following substituents and values are intended to provide representative examples of various aspects and embodiments of the invention. These representative values are intended to further define and illustrate such aspects and embodiments and are not intended to exclude other embodiments or to limit the scope of the invention. In this regard, the representation that a particular value or substituent is preferred is not intended in any way to exclude other values or substituents from the invention unless specifically indicated.

R¹ is selected from —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl, —C₁₋₃alkylene-SCH₃, —C₃₋₉cycloalkyl, and heteroaryl. In one embodiment, R¹ is —C₁₋₆alkyl, such as —CH₂CH(CH₃)₂. In another embodiment, R¹ is —C₂₋₆alkenyl, such as —CH₂CH═CH₂. In still another embodiment, R¹ is —C₂₋₆alkynyl, such as —C≡CH. In still another embodiment, R¹ is —C₁₋₃alkylene-SCH₃, such as —(CH₂)₂SCH₃. In still another embodiment, R¹ is —C₃₋₉cycloalkyl, such as cyclopropyl and cyclopentyl. The —C₃₋₉cycloalkyl group is optionally substituted with 1 to 5 R groups independently selected from —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, —C₃₋₆cycloalkyl, cyano, halo, —OR^(a), —SR^(a), —S(O)R^(a), —S(O)₂R^(a), and —NR^(b)R^(c); where each R^(a) is independently selected from H, —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, and —C₃₋₆cycloalkyl; and each R^(b) and R^(c) is independently selected from H, —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, and —C₃₋₆cycloalkyl. In one embodiment, the —C₃₋₉cycloalkyl group is unsubstituted. When present, each R group may be at any position of the —C₃₋₉cycloalkyl ring to which it is attached. When more than one R substituent is present, i.e., a is 2, 3, 4 or 5, the substituents can be on the same or on different carbon atoms. In one embodiment, R is independently selected from —C₁₋₄alkyl (e.g. methyl, ethyl, n-propyl, isopropyl), halo (e.g., fluoro or chloro) and —OR^(1a) (e.g., hydroxy, methoxy, ethoxy). Each of the aforementioned alkyl, alkenyl, alkynyl, and cycloalkyl groups in R may be substituted with 1 to 5 fluoro atoms. It is understood that when referring to these groups in R, reference is also made to any such groups that might be present in the R^(a), R^(b), and R^(c) moieties. For example, R¹ can be —C₁₋₄alkyl such as difluoromethyl, trifluoromethyl, and 2,2,2-trifluoroethyl, or —OR^(a), where R^(a) is difluoromethyl or trifluoromethyl.

In another embodiment, R¹ is heteroaryl, such as thiophene (including 2-thiophene and 3-thiophene).

R² is an aryl or heteroaryl group. In one particular embodiment, R² is an aryl group such as phenyl or naphthalenyl; in another embodiment Ar is phenyl. In one particular embodiment, R² is a heteroaryl group such as thiophene (including 2-thiophene and 3-thiophene). The aryl in R² may be substituted with 1 to 5 R groups independently selected from —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, —C₃₋₆cycloalkyl, cyano, halo, —OR^(a), —SR^(a), —S(O)R^(a), —S(O)₂R^(a), and —NR^(b)R^(c). Each R^(a) is independently selected from H, —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl and —C₃₋₆cycloalkyl. Each R^(b) and R^(c) is independently selected from H, —C₁₋₄alkenyl, —C₂₋₄alkynyl, and —C₃₋₆cycloalkyl. Each of the aforementioned alkyl, alkenyl, alkynyl, and cycloalkyl groups in R may be substituted with 1 to 5 fluoro atoms. It is understood that when referring to these groups in R², reference is also made to any such groups that might be present in the R^(a), R^(b), and R^(c) moieties. In one particular embodiment, R² is phenyl and is unsubstituted. In another embodiment, R² is phenyl and is substituted with 1 or 2 R groups independently selected from —C₁₋₄alkyl, (for example, —CH₃), halo (for example fluoro) and —OR^(a) (where R^(a) is H or —C₁₋₄alkyl such as —CH₃). In one particular embodiment, R² is phenyl and is substituted with 1 fluoro atom.

R³ is selected from H and —C₀₋₁alkylene-OH, where the alkylene group is optionally substituted with 1 to 5 fluoro atoms. In one embodiment, R³ is selected from H and —OH. In another embodiment, R³ is —OH. In yet another embodiment, R³ is —CH₂OH. Alternatively, when R¹ is —C₃₋₉cycloalkyl, R³ may form a double bond with the carbon atom on the —C₃₋₉cycloalkyl group, an embodiment which may be depicted as:

In one particular embodiment, R¹ is cyclopentyl and R³ forms a double bond with the carbon atom on the cyclopentyl group.

In yet another embodiment, —CR¹R² together form a group of formula:

In one such embodiment, R³ is H.

The nitrogen containing ring can have from 3 to 6 carbon atoms in the ring, and thus is depicted as:

This depiction is intended to include the following nitrogen containing rings:

In one particular embodiment, the nitrogen containing ring is:

The values for a are 0, 1, 2 or 3; and even more particularly 0 or 1. In one embodiment, a is 0.

When present, each R⁴ is independently selected from fluoro and —C₁₋₄alkyl. When more than one R⁴ substituent is present, i.e., a is 2 or 3, the substituents can be on the same or on different carbon atoms. Exemplary R⁴ groups include, but are not limited to, methyl, ethyl, and fluoro. The alkyl group in R⁴ may be substituted with 1 to 5 fluoro atoms. For example, R⁴ can be difluoromethyl or trifluoromethyl.

R⁵ is selected from —C₁₋₅alkyl and —C₀₋₁alkyleneC₃₋₅cycloalkyl. Each of the aforementioned alkyl, alkylene, and cycloalkyl groups in R⁵ may be substituted with 1 to 5 fluoro atoms. In one embodiment, R⁵ is —C₁₋₅alkyl such as —CH₃.

R⁶ is selected from —C₁₋₃alkyl, —C₁₋₂alkyleneC₃₋₇cycloalkyl, —C₀₋₄alkylene-OH, —C₁₋₂alkylene-C(O)O—C₁₋₄alkyl, and —C₁₋₂alkylene-C(O)NR^(6a)R^(6b). R^(6a) and R^(6b) are independently selected from H and —C₁₋₄alkyl. Exemplary —C₁₋₃alkyl groups include —CH₃, —CH₂CH₃, and —(CH₂)₂CH₃. Exemplary —C₁₋₂alkyleneC₃₋₇cycloalkyl groups include —CH₂-cyclopropyl. Exemplary —C₀₋₄alkylene-OH groups include —(CH₂)₂OH. Exemplary —C₁₋₂alkylene-C(O)O—C₁₋₄alkyl groups include —CH₂—C(O)OCH₃. Exemplary —C₁₋₂alkylene-C(O)NR^(6a)R^(6b) groups include —CH₂—C(O)NH₂. Alternately, R⁶ is taken with R⁵ to form —C₃₋₅alkylene-. Each of the aforementioned alkyl, alkylene, and cycloalkyl groups in R⁶ may be substituted with 1 to 5 fluoro atoms. It is understood that when referring to these groups in R⁶, reference is also made to any such groups that might be present in the R^(6a) and R^(6b) moieties.

Z is selected from a bond, —O—, —S—, —S(O)—, —SO₂—, —SO₂—NR^(Z1)—, —NR^(Z1)—SO₂—, —C(O)—, —OC(O)—, —C(O)O—, —NR^(Z1)C(O)—, —C(O)NR^(Z1)—, —NR^(Z2)—C(O)—NR^(Z3)—, —NR^(Z2)—C(S)—NR^(Z3)—, —CH(OH)—, and —C(═N—O—R^(Z4))—. In one embodiment, Z is selected from a bond, —O—, and —C(O)—. R^(Z1) is selected from H and —C₁₋₄alkyl. In one particular embodiment, R^(Z1) is hydrogen. R^(Z2) and R^(Z3) are independently selected from H, —C₁₋₄alkyl, and —C₃₋₆cycloalkyl. Alternately, R^(Z2) and R^(Z3) are taken together to form —C₂₋₄alkylene- or —C₂₋₃alkenylene-. In one particular embodiment, R^(Z2) and R^(Z3) are both hydrogen. R^(Z4) is selected from —C₁₋₄alkyl and benzyl. In one embodiment, R^(Z4) is —C₁₋₄alkyl such as —CH₃. In another embodiment, R^(Z4) is benzyl. Each of the aforementioned alkyl, alkylene, alkenylene, and cycloalkyl groups in Z may be substituted with 1 to 5 fluoro atoms. It is understood that when referring to these groups in Z, reference is made to such groups that are present in the R^(Z1), R^(Z2), and R^(Z3) moieties.

The linker connecting the nitrogen-containing ring to the quaternary nitrogen may be a bond (0 carbon atoms) or may have 1 carbon atom, and thus may be designated as —(CH₂)₀₋₁— or —C₀₋₁alkylene-. In one particular embodiment, this linker is a bond. In another embodiment, this linker contains one carbon atom.

The linker connecting the quaternary nitrogen to the Z moiety contains from 1-4 carbon atoms, and thus may be designated as —(CH₂)₁₋₄— or —C₁₋₄alkylene-. Each —CH₂— group in —(CH₂)₁₋₄— is optionally substituted with 1 or 2 substituents independently selected from —C₁₋₂alkyl, —OH, fluoro, and phenyl. In one embodiment, one —CH₂— group in —(CH₂)₁₋₄— is optionally substituted with —OH or phenyl.

These two linkers, in combination with the quaternary nitrogen and the Z moiety, can be depicted as —(CH₂)₀₋₁—N(R⁵R⁶)—(CH₂)₁₋₄—Z—, and forming the linking moiety between the nitrogen-containing ring and the Q moiety. In specific embodiments, —(CH₂)₀₋₁—N(R⁵R⁶)—(CH₂)₁₋₄αZα is selected from one of the following: —N(CH₃)₂—CH₂—, —N(CH₃)₂—(CH₂)₂—, —N(CH₃)₂—(CH₂)₃—, —N(CH₃)₂—(CH₂)₄—, —N(CH₃)₂—CH₂—CH(phenyl)-, —N(CH₃)₂—CH₂—CH(OH)—, —N(CH₃)₂—CH₂—C(O)—, —N(CH₃)₂—(CH₂)₂—O—, —N(CH₃)₂—(CH₂)₃—O—, —N(CH₃)₂—(CH₂)₄—O—, —CH₂—N(CH₃)₂—CH₂—, —CH₂—N(CH₃)₂—(CH₂)₂—, —CH₂—N(CH₃)₂—(CH₂)₃—, —N(CH₃)(CH₂CH₃)—(CH₂)₂—, —N(CH₃)—[(CH₂)₂CH₃]—(CH₂)₂—, —N(CH₃)(CH₂-cyclopropyl)-(CH₂)₂—, —N(CH₃)(CH₂CH₂OH)—(CH₂)₂—, —N(CH₃)[CH₂C(O)OCH₃]—(CH₂)₂—, and —N(CH₃)[CH₂C(O)NH₂]—(CH₂)₂—.

Q is an aryl or heteroaryl group, as those term are defined herein. In one embodiment Q is an aryl group such as phenyl. In another embodiment, Q is a heteroaryl group selected from thienyl (e.g., thiophen-2-yl or thiophen-3-yl), furanyl, pyrrolyl (e.g., pyrrol-1-yl), pyrazolyl, benzo[1,3]dioxolyl, indolyl (e.g., 1H-indol-3-yl), and tetrazolyl (e.g., 1H-tetrazol-5-yl), and piperidinyl (e.g., piperidin-4-yl).

When Q is an aryl group, it may be substituted with 1 to 5 R^(Q) groups independently selected from halo, —C₁₋₄alkyl, —C₀₋₄alkylene-OH, cyano, —C₀₋₂alkylene-COOH, —C(O)O—C₁₋₄alkyl, —O—C₁₋₄alkyl, —S—C₁₋₄alkyl, —NH—C(O)—C₁₋₄alkyl, —N-di-C₁₋₄alkyl, and —N⁺(O)O. In another embodiment, each R^(Q) is independently selected from halo, C₁₋₄alkyl, —C₀₋₄alkylene-OH, cyano, —C₀₋₂alkylene-COOH, —C(O)O—C₁₋₄alkyl, and —O—C₁₋₄alkyl. Exemplary halo groups include fluoro, chloro, and bromo. Exemplary —C₁₋₄alkyl groups include —CH₃ and —C(CH₃)₃, as well as fluoro-substituted alkyl groups such as —CF₃. Exemplary —C₀₋₄alkylene-OH groups include —OH and —(CH₂)₂—OH. Exemplary —C₀₋₂alkylene-COOH groups include —COOH (carboxy) and —CH₂COOH (carboxymethyl). Exemplary —C(O)O—C₁₋₄alkyl groups include —C(O)OCH₃ (methoxycarbonyl). Exemplary —O—C₁₋₄alkyl groups include —OCH₃, as well as fluoro-substituted alkoxy groups such as —OCHF₂ (difluoromethoxy). Exemplary —S—C₁₋₄alkyl groups include —S—CH₃. Exemplary —NH—C(O)—C₁₋₄alkyl groups include —NH—C(O)—CH₃. Exemplary —N-di-C₁₋₄alkyl groups include —N(CH₃)₂.

When more than one R^(Q) substituent is present, the substituents can be on the same or on different ring atoms. Each of the aforementioned alkyl and alkylene groups in Q may be substituted with 1 to 5 fluoro atoms. It is understood that when referring to these groups in Q, reference is made to such groups that are present in the R^(Q) moiety. In one embodiment, Q is unsubstituted. In another embodiment, Q is substituted with one R^(Q) group; and in another embodiment, R^(Q) is selected from halo, —C₀₋₄alkylene-OH, cyano, —C₀₋₂alkylene-COOH, —C(O)O—C₁₋₄alkyl, and —O—C₁₋₄alkyl, and —N⁺(O)O. In another embodiment, Q is substituted with two R^(Q) groups; and in another embodiment, each R^(Q) is independently selected from halo, —C₁₋₄alkyl, —C₀₋₄alkylene-OH, —C(O)O—C₁₋₄alkyl, and —O—C₁₋₄alkyl.

X⁻ is an anion of a pharmaceutically acceptable acid. The term “anion of a pharmaceutically acceptable acid” is used to refer to an anionic counterion of a pharmaceutically acceptable acid. Examples of pharmaceutically acceptable inorganic acids include, by way of illustration and not limitation, boric, carbonic, hydrohalic (hydrobromic, hydrochloric, hydrofluoric or hydroiodic), nitric, phosphoric, sulfamic and sulfuric acids, and hydroxide. Examples of pharmaceutically acceptable organic acids include, by way of illustration and not limitation, aliphatic hydroxyl acids (e.g., citric, gluconic, glycolic, lactic, lactobionic, malic, and tartaric acids), aliphatic monocarboxylic acids (e.g., acetic, butyric, formic, propionic and trifluoroacetic acids), aromatic carboxylic acids (e.g., benzoic, p-chlorobenzoic, diphenylacetic, gentisic, hippuric, and triphenylacetic acids), amino acids (e.g., aspartic and glutamic acids), aromatic hydroxyl acids (e.g., o-hydroxybenzoic, p-hydroxybenzoic, 1-hydroxynaphthalene-2-carboxylic and 3-hydroxynaphthalene-2-carboxylic acids), ascorbic, dicarboxylic acids (e.g., fumaric, maleic, oxalic and succinic acids), glucoronic, mandelic, mucic, nicotinic, orotic, pamoic, pantothenic, sulfonic acids (e.g., benzenesulfonic, camphosulfonic, edisylic, ethanesulfonic, isethionic, methanesulfonic, naphthalenesulfonic, naphthalene-1,5-disulfonic, naphthalene-2,6-disulfonic and p-toluenesulfonic acids), xinafoic acid, and the like. In one embodiment, the pharmaceutically acceptable acid is selected from acetic, benzenesulfonic, benzoic, butyric, p-chlorobenzoic, citric, diphenylacetic, formic, hydrobromic, hydrochloric, hydrofluoric, hydroiodic, o-hydroxybenzoic, p-hydroxybenzoic, 1-hydroxynaphthalene-2-carboxylic, 3-hydroxynaphthalene-2-carboxylic, lactic, malic, maleic, methanesulfonic, nitric, phosphoric, propionic, succinic, sulfuric, tartaric, trifluoroacetic, and triphenylacetic acids. In another embodiment the pharmaceutically acceptable acid is selected from hydrobromic, hydroiodic, and trifluoroacetic acids. In one embodiment, the anion is selected from acetate, benzenesulfonate, benzoate, bromide, butyrate, chloride, p-chlorobenzoate, citrate, diphenylacetate, formate, fluoride, o-hydroxybenzoate, p-hydroxybenzoate, 1-hydroxynaphthalene-2-carboxylate, 3-hydroxynaphthalene-2-carboxylate, iodide, lactate, malate, maleate, methanesulfonate, nitrate, phosphate, propionate, succinate, sulfate, tartrate, trifluoroacetate, bi- and triphenylacetate. In yet another embodiment, the anion is selected from bromide, iodide and trifluoroacetate.

In one embodiment the compounds of the invention have formula I or II and: R¹ is selected from —C₁₋₆alkyl, —C₂₋₆alkenyl, —C₂₋₆alkynyl, —C₁₋₃alkylene-SCH₃, —C₃₋₉cycloalkyl, and heteroaryl; R² is an aryl or heteroaryl group; R³ is selected from H and —C₀₋₁alkylene-OH; or when R¹ is —C₃₋₉cycloalkyl, R³ can form a double bond with the carbon atom on the —C₃₋₉cycloalkyl group; or —CR¹R² together form a group of formula:

a is 0; R⁵ is —C₁₋₅alkyl; R⁶ is selected from —C₁₋₃alkyl, —C₁₋₂alkyleneC₃₋₇cycloalkyl, —C₀₋₄alkylene-OH, —C₁₋₂alkylene-C(O)O—C₁₋₄alkyl, and —C₁₋₂alkylene-C(O)NH₂; Z is selected from a bond, —O—, and —C(O)—; Q is an aryl or heteroaryl group; wherein the aryl in R² is optionally substituted with 1 to 2 R groups independently selected from —C₁₋₄alkyl, halo, and —OR^(a); where each R^(a) is independently selected from H and —C₁₋₄alkyl; the aryl in Q is optionally substituted with 1 to 2 R^(Q) groups independently selected from halo, —C₁₋₄alkyl, —C₀₋₄alkylene-OH, cyano, —C₀₋₂alkylene-COOH, —C(O)O—C₁₋₄alkyl, —O—C₁₋₄alkyl, and —N⁺(O)O; each alkyl in R^(Q) is optionally substituted with 1 to 5 fluoro atoms; and one —CH₂— group in —(CH₂)₁₋₄— is optionally substituted with a group selected from —OH and phenyl.

In another embodiment the compounds of the invention have formula I or II and: R¹ is selected from —CH₂CH(CH₃)₂, —CH₂CH═CH₂, cyclopropyl, and cyclopentyl, when R² is phenyl and R³ is —OH; or R¹ is-cyclopropyl when R² is phenyl and R³ is H; or R¹ is cyclopentyl when R² is phenyl and R³ forms a double bond with the carbon atom on the cyclopentyl group; or R¹ is cyclopentyl or thiophenyl, when R² is thiophenyl and R³ is —OH; or —CR¹R² together form a group of formula:

and: a is 0; the linker —(CH₂)₀₋₁—N(R⁵R⁶)—(CH₂)₁₋₄—Z— is selected from: —N(CH₃)₂—(CH₂)₂—, —N(CH₃)(CH₂CH₃)—(CH₂)₂—, and —N(CH₃)₂—CH₂—C(O)—; Q is selected from phenyl, thiophen-2-yl, thiophen-3-yl, and benzo[1,3]dioxol-5-yl; wherein the phenyl in R² is optionally substituted with 1 to 2 R groups independently selected from —CH₃, fluoro, —OH, and —OCH₃; the phenyl in Q is optionally substituted with 1 to 2 R^(Q) groups independently selected from fluoro, bromo, —CH₃, and —OH.

In another embodiment of the invention, the quaternary ammonium compound of formula II is the species embodied in formula IIa:

where R¹⁻⁶, a, Z, Q and X⁻ are as defined for formula I; and pharmaceutically acceptable salts thereof. In one particular embodiment, R′ is selected from —CH₂CH(CH₃)₂, —CH₂CH═CH₂, —(CH₂)₂SCH₃, cyclopropyl, cyclopentyl, and thiophenyl; R² is selected from phenyl and thiophenyl; R³ is selected from H and —C₀₋₁alkylene-OH; or when R¹ is cyclopentyl, R³ can form a double bond with the carbon atom on the cyclopentyl group; or —CR¹R² together form a group of formula:

a is 0; R⁵ is —CH₃; R⁶ is selected from —CH₃, —CH₂CH₃, —(CH₂)₂CH₃, —CH₂-cyclopropyl, —(CH₂)₂OH, —CH₂—C(O)OCH₃, and —CH₂—C(O)NH₂; Z is selected from a bond, —O—, and —C(O)—; Q is selected from phenyl, 1H-indol-3-yl, thiophen-2-yl, thiophen-3-yl, benzo[1,3]dioxol-5-yl, pyrrol-1-yl, 1H-tetrazol-5-yl, and piperidin-4-yl; wherein the phenyl in R² is optionally substituted with 1 to 2 R groups independently selected from —CH₃, fluoro, —OH, and —OCH₃; the phenyl in Q is optionally substituted with 1 to 2 R^(Q) groups independently selected from fluoro, chloro, bromo, —CH₃, —CF₃, —C(CH₃)₃, —OH, —(CH₂)₂—OH, cyano, —COOH, —CH₂COOH, C(O)OCH₃, —OCH₃, —OCHF₂, and —N⁺(O)O; and one —CH₂— group in —(CH₂)₁₋₄— is optionally substituted with 1 or 2 substituents selected from —OH and phenyl.

In another embodiment of the invention, the quaternary ammonium compound of formula II is the species embodied in formula IIb:

where R, R¹, R³, R⁵, R⁶, Z, Q and X⁻ are as defined for formula I; and pharmaceutically acceptable salts thereof. In one particular embodiment, R¹ is selected from —CH₂CH(CH₃)₂, —CH₂CH═CH₂, —C≡CH, —(CH₂)₂SCH₃, cyclopropyl, and cyclopentyl; R³ is selected from H—C₀₋₁alkylene-OH; or when R¹ is cyclopentyl, R³ can form a double bond with the carbon atom on the cyclopentyl group; R⁵ is —CH₃; R⁶ is selected from —CH₃, —CH₂CH₃, —(CH₂)₂CH₃, —CH₂-cyclopropyl, —(CH₂)₂OH, —CH₂—C(O)OCH₃, and —CH₂—C(O)NH₂; Z is selected from a bond, —O—, and —C(O)—; Q is selected from phenyl, 1H-indol-3-yl, thiophen-2-yl, thiophen-3-yl, benzo[1,3]dioxol-5-yl, pyrrol-1-yl, 1H-tetrazol-5-yl, and piperidin-4-yl; wherein R is independently selected from —CH₃, fluoro, —OH, and —OCH₃; the phenyl in Q is optionally substituted with 1 to 2 R^(Q) groups independently selected from fluoro, chloro, bromo, —CH₃, —CF₃, —C(CH₃)₃, —OH, —(CH₂)₂—OH, cyano, —COOH, —CH₂COOH, C(O)OCH₃, —OCH₃, —OCHF₂, and —N⁺(O)O; and one —CH₂— group in —(CH₂)₁₋₄— is optionally substituted with 1 substituent selected from —C₁₋₂alkyl, —OH and phenyl.

In another embodiment of the invention, the quaternary ammonium compound of formula II is the species embodied in formula IIc:

where R, R¹, R³, R⁵, R⁶, Z, R^(Q) and X⁻ are as defined for formula I; and pharmaceutically acceptable salts thereof. In one particular embodiment, R¹ is selected from —CH₂CH(CH₃)₂, —CH₂CH═CH₂, —C≡CH, —(CH₂)₂SCH₃, cyclopropyl, and cyclopentyl; R³ is selected from H and —C₀₋₁alkylene-OH; or when R¹ is cyclopentyl, R³ can form a double bond with the carbon atom on the cyclopentyl group; R⁵ is —CH₃; R⁶ is selected from —CH₃, —CH₂CH₃, —(CH₂)₂CH₃, —CH₂-cyclopropyl, —(CH₂)₂OH, —CH₂—C(O)OCH₃, and —CH₂—C(O)NH₂; Z is selected from a bond, —O—, and —C(O)—; wherein R is independently selected from —CH₃, fluoro, —OH, and —OCH₃; R^(Q) is independently selected from fluoro, chloro, bromo, —CH₃, —CF₃, —C(CH₃)₃, —OH, —(CH₂)₂—OH, cyano, —COOH, —CH₂COOH, C(O)OCH₃, —OCH₃, —OCHF₂, and —N⁺(O)O; and one —CH₂— group in —(CH₂)₁₋₄— is optionally substituted with 1 substituent selected from —C₁₋₂alkyl, —OH and phenyl.

In another embodiment of the invention, the quaternary ammonium compound of formula II is the species embodied in formula IId:

where R³, Z, R^(Q) and X⁻ are as defined for formula I; and pharmaceutically acceptable salts thereof. In one particular embodiment, R³ is —OH; Z is a bond; and R^(Q) is independently selected from fluoro and —OH.

In another embodiment of the invention, the quaternary ammonium compound of formula II is the species embodied in formula IIe:

where R³, Z, Q and X⁻ are as defined for formula I; and pharmaceutically acceptable salts thereof. In one particular embodiment, R³ is —OH; Z is a bond; Q is phenyl or benzo[1,3]dioxol-5-yl; and the phenyl in Q is optionally substituted with 1 R^(Q) group selected from fluoro and —CH₃.

In another embodiment of the invention, the quaternary ammonium compound of formula II is the species embodied in formula IIf:

where Z, Q and X⁻ are as defined for formula I; and pharmaceutically acceptable salts thereof. In one particular embodiment, R³ is H; Z is a bond; Q is phenyl, thiophen-2-yl, or thiophen-3-yl; and the phenyl in Q is optionally substituted with 1 R^(Q) group selected from fluoro and —OH.

A particular group of compounds of formula I are those disclosed in U.S. Provisional Application No. 60/925,951, filed on Apr. 24, 2007. This group includes compounds of formula (I′):

in salt or zwitterionic form, wherein: a′ is 0 or an integer of from 1 to 5; each R^(1′) is independently selected from —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, —C₃₋₆cycloalkyl, cyano, halo, —OR^(1a), —SR^(1a), —S(O)R^(1a), —S(O)₂R^(1a), and —NR^(1b)R^(1c); where each R^(1a) is independently selected from H, —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, and —C₃₋₆cycloalkyl; and each R^(1b) and R^(1c) is independently selected from H, —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, and —C₃₋₆cycloalkyl; Ar′ is an aryl group; R^(3′) is selected from H and —C₀₋₁alkylene-OH; or R³ forms a double bond with the carbon atom on the —C₅₋₉ cycloalkyl group; b′ is 0 or an integer of from 1 to 3; each R^(4′) is independently selected from fluoro and —C₁₋₄alkyl; R^(5′) is selected from —C₁₋₅alkyl and —C₀₋₁alkyleneC₃₋₅cycloalkyl; R^(6′) is selected from —C₁₋₃alkyl, —C₁₋₂alkyleneC₃₋₇cycloalkyl, —C₀₋₄alkylene-OH, —C₁₋₂alkylene-C(O)O—C₁₋₄alkyl, and —C₁₋₂alkylene-C(O)NR^(6a)R^(6b); where R^(6a) and R^(6b) are independently selected from H and —C₁₋₄alkyl; or R⁶ is taken with R⁵ to form —C₃₋₅alkylene-; Z′ is selected from a bond, —O—, —S—, —S(O)—, —SO₂—, —SO₂—NR^(Z1)—, —NR^(Z1)—SO₂—, —C(O)—, —OC(O)—, —C(O)O—, —NR^(Z1)C(O)—, —C(O)NR^(Z1)—, —NR^(Z2)—C(O)—NR^(Z3)—, —NR^(Z2)—C(S)—NR^(Z3)—, —CH(OH)—, and —C(═N—O—R^(Z4))—; where R^(Z1) is selected from H and —C₁₋₄alkyl; R^(Z2) and R^(Z3) are independently selected from H, —C₁₋₄alkyl, and —C₃₋₆cycloalkyl, or R^(Z2) and R^(Z3) are taken together to form —C₂₋₄alkylene- or —C₂₋₃alkenylene-; and R^(Z4) is selected from —C₁₋₄alkyl and benzyl; Q′ is an aryl or heteroaryl group; wherein Ar′ is optionally substituted with 1 to 5 R^(2′) groups independently selected from —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, —C₃₋₆cycloalkyl, cyano, halo, —OR^(2a), —SR^(2a), —S(O)R^(2a), —S(O)₂R^(2a), and —NR^(2b)R^(2c); where each R^(2a) is independently selected from H, —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, and —C₃₋₆cycloalkyl; and each R^(2b) and R^(2c) is independently selected from H, —C₁₋₄alkyl, —C₂₋₄alkenyl, —C₂₋₄alkynyl, and —C₃₋₆cycloalkyl; wherein Q′ is optionally substituted with 1 to 5 R^(Q) groups independently selected from halo, —C₁₋₄alkyl, —C₀₋₄alkylene-OH, cyano, —C₀₋₂alkylene-COOH, —C(O)O—C₁₋₄alkyl, —O—C₁₋₄alkyl, —S—C₁₋₄alkyl, —NH—C(O)—C₁₋₄alkyl, —N-di-C₁₋₄alkyl, and —N⁺(O)O; wherein each alkyl, alkylene, alkenyl, alkenylene, alkynyl and cycloalkyl group in R^(1′-6′), Z′ and Q′ is optionally substituted with 1 to 5 fluoro atoms; and each —CH₂— group in —(CH₂)₁₋₄— is optionally substituted with 1 or 2 substituents independently selected from —C₁₋₂alkyl, —OH, fluoro, and phenyl; and pharmaceutically acceptable salts thereof.

In addition, particular compounds of formula I that are of interest include those set forth in the Examples below, as well as the pharmaceutically acceptable salts thereof

DEFINITIONS

When describing the compounds, compositions, methods and processes of the invention, the following terms have the following meanings unless otherwise indicated. Additionally, as used herein, the singular forms “a,” “an” and “the” include the corresponding plural forms unless the context of use clearly dictates otherwise. The terms “comprising”, “including,” and “having” are intended to be inclusive and mean that there may be additional elements other than the listed elements.

The term “alkyl” means a monovalent saturated hydrocarbon group which may be linear or branched. Unless otherwise defined, such alkyl groups typically contain from 1 to 10 carbon atoms and include, for example —C₁₋₂alkyl, —C₁₋₃alkyl, —C₁₋₄alkyl, —C₁₋₅alkyl, and —C₁₋₆alkyl. Representative alkyl groups include, by way of example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl and the like.

When a specific number of carbon atoms is intended for a particular term used herein, the number of carbon atoms is shown preceding the term as subscript. For example, the term “—C₁₋₄alkyl” means an alkyl group having from 1 to 4 carbon atoms, where the carbon atoms are in any acceptable configuration.

The term “alkylene” means a divalent saturated hydrocarbon group that may be linear or branched. Unless otherwise defined, such alkylene groups typically contain from 1 to 10 carbon atoms and include, for example, —C₀₋₁alkylene-, —C₀₋₂alkylene-, —C₀₋₄alkylene-, —C₀₋₅alkylene-, —C₁₋₂alkylene-, —C₁₋₄alkylene-, —C₂₋₄alkylene-, —C₂₋₅alkylene-, —C₃₋₅alkylene-, and —C₃₋₆alkylene-. Representative alkylene groups include, by way of example, methylene, ethane-1,2-diyl (“ethylene”), propane-1,2-diyl, propane-1,3-diyl, butane-1,4-diyl, pentane-1,5-diyl and the like. It is understood that when the alkylene term include zero carbons such as —C₀₋₁alkylene- or —C₀₋₅alkylene-, such terms are intended to include a single bond.

The term “alkenyl” means a monovalent unsaturated hydrocarbon group which may be linear or branched and which has at least one, and typically 1, 2 or 3, carbon-carbon double bonds. Unless otherwise defined, such alkenyl groups typically contain from 2 to 10 carbon atoms and include, for example, —C₂₋₄alkenyl and —C₂₋₆alkenyl. Representative alkenyl groups include, by way of example, ethenyl, n-propenyl, isopropenyl, n-but-2-enyl, n-hex-3-enyl and the like. The term “alkenylene” means a divalent alkenyl group, and exemplary alkenylene groups include —C₂₋₃alkenylene-.

The term “alkynyl” means a monovalent unsaturated hydrocarbon group which may be linear or branched and which has at least one, and typically 1, 2 or 3, carbon-carbon triple bonds. Unless otherwise defined, such alkynyl groups typically contain from 2 to 10 carbon atoms and include, for example, —C₂₋₄alkynyl and —C₂₋₆alkynyl. Representative alkynyl groups include, by way of example, ethynyl, n-propynyl, n-but-2-ynyl, n-hex-3-ynyl and the like.

The term “amino-protecting group” means a protecting group suitable for preventing undesired reactions at an amino group. Representative amino-protecting groups include, but are not limited to, tert-butoxycarbonyl (BOC), trityl (Tr), benzyloxycarbonyl (Cbz), 9-fluorenylmethoxycarbonyl (Fmoc), formyl, trimethylsilyl (TMS), tert-butyldimethylsilyl (TBS), and the like.

The term “aryl” means a monovalent aromatic hydrocarbon having a single ring (i.e., phenyl) or fused rings (i.e., naphthalene). Unless otherwise defined, such aryl groups typically contain from 6 to 10 carbon ring atoms and include, for example, —C₆₋₁₀aryl. Representative aryl groups include, by way of example, phenyl and naphthalene-1-yl, naphthalene-2-yl, and the like.

The term “cycloalkyl” means a monovalent saturated carbocyclic hydrocarbon group. Unless otherwise defined, such cycloalkyl groups typically contain from 3 to 10 carbon atoms and include, for example, —C₃₋₅cycloalkyl, —C₃₋₆cycloalkyl, —C₃₋₇cycloalkyl, and —C₅₋₉ cycloalkyl. Representative cycloalkyl groups include, by way of example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and the like.

The term “divalent hydrocarbon group” means a divalent hydrocarbon group which is composed primarily of carbon and hydrogen atoms and which optionally contains one or more heteroatoms. Such divalent hydrocarbon groups may be branched or unbranched, saturated or unsaturated, acyclic or cyclic, aliphatic or aromatic, or combinations thereof. The divalent hydrocarbon group can optionally contain heteroatoms incorporated into the hydrocarbon chain or as substituents attached to the hydrocarbon chain.

The term “halo” means fluoro, chloro, bromo and iodo.

The term “heteroaryl” means a monovalent aromatic group having a single ring or two fused rings and containing in the ring at least one heteroatom (typically 1 to 3 heteroatoms) selected from nitrogen, oxygen or sulfur. Unless otherwise defined, such heteroaryl groups typically contain from 5 to 10 total ring atoms and include, for example, —C₂₋₉heteroaryl. Representative heteroaryl groups include, by way of example, monovalent species of pyrrole, imidazole, thiazole, oxazole, furan, thiophene, triazole, pyrazole, isoxazole, isothiazole, pyridine, pyrazine, pyridazine, pyrimidine, triazine, indole, benzofuran, benzothiophene, benzimidazole, benzthiazole, quinoline, isoquinoline, quinazoline, quinoxaline and the like, where the point of attachment is at any available carbon or nitrogen ring atom.

The term “leaving group” means a functional group or an atom that can be displaced by another functional group or atom in a substitution reaction, such as a nucleophilic substitution reaction. By way of example, representative leaving groups include, but are not limited to, chloro, bromo and iodo groups; sulfonic ester groups, such as mesylate, tosylate, brosylate, nosylate and the like; and acyloxy groups, such as acetoxy, trifluoroacetoxy and the like.

The term “pharmaceutically acceptable” refers to a material that is not biologically or otherwise undesirable. For example, the term “pharmaceutically acceptable carrier” refers to a material that can be incorporated into a composition and administered to a patient without causing undesirable biological effects or interacting in a deleterious manner with other components of the composition. Such pharmaceutically acceptable materials typically have met the required standards of toxicological and manufacturing testing, and include those materials identified as suitable inactive ingredients by the U.S. Food and Drug administration.

The term “solvate” means a complex or aggregate formed by one or more molecules of a solute, e.g., a compound of formula I or a pharmaceutically acceptable salt thereof, and one or more molecules of a solvent. Such solvates are typically crystalline solids having a substantially fixed molar ratio of solute and solvent. Representative solvents include, by way of example, water, methanol, ethanol, isopropanol, acetic acid and the like. When the solvent is water, the solvate formed is a hydrate.

The term “therapeutically effective amount” means an amount sufficient to effect treatment when administered to a patient in need of treatment. In particular, an “effective” amount is that amount needed to obtain the desired result, and a “therapeutically effective” amount is that amount needed to obtain the desired therapeutic effect. For example, for antagonizing a muscarinic receptor, an “effective amount” is a muscarinic receptor-antagonizing amount. Similarly, a therapeutically effective amount for treating chronic obstructive pulmonary disease (COPD) is that amount that will achieve the desired therapeutic result, which may be disease prevention, amelioration, suppression or alleviation.

The term “treating” or “treatment” as used herein means the treating or treatment of a disease or medical condition (such as COPD or asthma) in a patient, such as a mammal (particularly a human) that includes: (a) preventing the disease or medical condition from occurring, i.e., prophylactic treatment of a patient; (b) ameliorating the disease or medical condition, i.e., eliminating or causing regression of the disease or medical condition in a patient; (c) suppressing the disease or medical condition, i.e., slowing or arresting the development of the disease or medical condition in a patient; or (d) alleviating the symptoms of the disease or medical condition in a patient. For example, the term “treating COPD” would include preventing COPD from occurring, ameliorating COPD, suppressing COPD, and alleviating the symptoms of COPD. The term “patient” is intended to include those animals, such as humans, that are in need of treatment or disease prevention, that are presently being treated for disease prevention or treatment of a specific disease or medical condition, as well as test subjects in which compounds of the invention are being evaluated or being used in a assay, for example an animal model.

All other terms used herein are intended to have their ordinary meaning as understood by those of ordinary skill in the art to which they pertain.

General Synthetic Procedures

Compounds of the invention can be prepared from readily available starting materials using the following general methods, the procedures set forth in the Examples, or by using other methods, reagents, and starting materials that are known to those of ordinary skill in the art. Although the following procedures may illustrate a particular embodiment of the invention, it is understood that other embodiments of the invention can be similarly prepared using the same or similar methods or by using other methods, reagents and starting materials known to those of ordinary skill in the art. It will also be appreciated that where typical or preferred process conditions (i.e., reaction temperatures, times, mole ratios of reactants, solvents, pressures, etc.) are given, other process conditions can also be used unless otherwise stated. While optimum reaction conditions will typically vary depending on various reaction parameters such as the particular reactants, solvents and quantities used, those of ordinary skill in the art can readily determine suitable reaction conditions using routine optimization procedures.

Additionally, as will be apparent to those skilled in the art, conventional protecting groups may be necessary or desired to prevent certain functional groups from undergoing undesired reactions. The choice of a suitable protecting group for a particular functional group as well as suitable conditions and reagents for protection and deprotection of such functional groups are well-known in the art. Functional groups that may be protected so as to prevent undesired reactions include, by way of example, carboxy groups, amino groups, hydroxyl groups, thiol groups, carbonyl groups and the like. Representative carboxy-protecting groups include, but are not limited to, esters, such as methyl, ethyl, t-butyl, benzyl (Bn), p-methoxybenzyl (PMB), 9-fluroenylmethyl (Fm), trimethylsilyl (TMS), t-butyldimethylsilyl (TBS), diphenylmethyl (benzhydryl, DPM) and the like; amides and hydrazides. Representative protecting groups for amino groups include carbamates (such as tert-butoxycarbonyl) and amides. Representative hydroxyl-protecting groups include, but are not limited to, silyl groups including triC₁₋₆alkylsilyl groups, such as trimethylsilyl (TMS), triethylsilyl (TES), t-butyldimethylsilyl (TBS) and the like; esters (acyl groups) including C₁₋₆alkanoyl groups, such as formyl, acetyl and the like; arylmethyl groups, such as benzyl (Bn), p-methoxybenzyl (PMB), 9-fluorenylmethyl (Fm), diphenylmethyl (benzhydryl, DPM) and the like; and ethers. Representative protecting groups for thiol groups include thioethers and thioesters. Representative protecting groups for carbonyl groups include acetals and ketals. Protecting groups other than those described herein may be used, if desired. For example, numerous protecting groups, and their introduction and removal, are described in T. W. Greene and G. M. Wuts, Protecting Groups in Organic Synthesis, Third Edition, Wiley, New York, 1999, and references cited therein.

By way of illustration, compounds of formula I can be prepared by one or more of the following exemplary processes: (a) reacting a compound of formula 1 with a compound of formula 2:

or reacting a compound of formula 1′ with a compound of formula 2′:

where L¹ represents a leaving group, to produce a compound of formula 3:

and reacting the compound of formula 3 with an organic substrate containing an R⁶ group; or (b) reacting a compound of formula 4:

with a compound of formula 2; or (c) reacting a compound of formula 4 with a compound of formula 5:

where L² represents a leaving group and A is defined below, to produce a compound of formula 6:

and reacting the compound of formula 6 with a compound of formula 7: B-Q  (7) where Z, A and B are defined as set forth in the following table, and L³ represents a leaving group:

Z A B bond —CH₃ L³— —O— —L³ HO— —S— —L³ HS— —SO₂—NR^(Z1)— —SO₂—OH or —SO₂Cl R^(Z1)HN— —NR^(Z1)—SO₂— —NHR^(Z1) HOO₂S— —OC(O)— —OH HO(O)C— —C(O)O— —C(O)OH or —C(O)Cl HO— —NR^(Z1)C(O)— —NHR^(Z1) HO(O)C— or Cl(O)C— —NR^(Z2)—C(O)—NR^(Z3)—, —N═C═O H₂N— where R^(Z2) and R^(Z3) are H NR^(Z2)—C(S)—NR^(Z3)—, where —N═S═O H₂N— R^(Z2) and R^(Z2) are H and recovering the product in salt or zwitterionic form.

The resulting reaction product, a compound of formula I, is a quaternary ammonium compound. This compound can be crystallized by first converting the compound to the appropriate counterion form, then crystallizing the compound in a suitable solvent. Such crystals are quaternary ammonium salts.

In these reactions, depending upon the particular substituents present, one or more protecting groups may be employed. If such protecting groups are used, they are removed using conventional procedures to provide the compound of formula I.

Process (a)

In process (a), the reaction between the compounds (1) and (2), the leaving group represented by L¹ can be, for example, halo, such as chloro, bromo or iodo, or a sulfonic ester group, such as mesylate or tosylate. In one embodiment, L¹ is bromo. The reaction is conveniently performed in the presence of a base, for example, a tertiary amine such as diisopropylethylamine. Convenient solvents include nitriles, such as acetonitrile, dimethylformamide (DMF), and dimethylacetamide (DMA). The reaction is conveniently conducted at a temperature in the range of from 0° C. to 100° C. The reaction product is then isolated using conventional procedures, such as extraction, recrystallization, chromatography and the like.

Compound (3), the free base form of the desired product, is dissolved in a suitable solvent then contacted with an organic substrate. Exemplary solvents include toluene, DMA, and CH₃CN. The organic substrate is typically a pharmaceutically acceptable acid such as an organic halide. The substrate contains an R⁶ group, for example, —C₁₋₆alkyl which may be substituted with 1-5 fluoro atoms, and a leaving group, examples of which include halides such as iodide or bromide. Exemplary substrates include methyl iodide, methyl bromide, ethyl iodide, propyl iodide, benzyl bromide and benzyl iodide.

In some situations, process (a) can be followed by a second reaction to yield a different compound of formula I. For example, compounds where Z is —S(O)— or —SO₂— can be made by forming a compound of formula I where Z is —S—, and subjecting such compound to an oxidation reaction. In addition, compounds where Z is —C(═N—O—R^(Z4))— can be made by forming a compound of formula I where Z is —C(O)—, and subjecting such compound to an imine formation reaction with H₂N—O—R^(Z4).

Compound (1) is generally known in the art or can be prepared from commercially available starting materials and reagents using well-known procedures. For example, compound (1) may be prepared by the following reaction:

in which P¹ represents an amino-protecting group, such as a benzyl group. Benzyl groups are conveniently removed by reduction, for example, using a hydrogen or ammonium formate and a Group VIII metal catalyst, such as palladium. Optionally, this reaction is conducted in the presence of an acid, such as formic acid, acetic acid, hydrochloric acid, hydrobromic acid, sulfuric acid and the like. Examples of compound (1′) include (R)-cyclopentylhydroxyphenyl acetic acid, 9H-Xanthene-9-carboxylic acid, and α-cyclopentylphenyl acetic acid. These compounds are commercially available or can be readily prepared, and exemplary preparation techniques are described in the examples section.

Compound (2) is generally known and commercially available, or can be prepared from readily available starting materials using well-known synthetic methods. Examples of compound (2) include 1-bromo-2-phenylethane, 3-(2-bromoethyl)phenol, 4-(2-bromoethyl)phenol, and 1-(2-bromoethyl)-2-fluorobenzene.

Alternately, compound (3) can be produced by coupling compounds (1′) and (2′) under conventional amide bond-forming conditions. Compound (2′) is generally known in the art or can be prepared from commercially available starting materials and reagents using well-known procedures. For example, compound (2′) may be prepared by the following reaction:

in which P¹ represents an amino-protecting group L¹ represents a leaving group.

Process (b)

In process (b), the reaction between the compounds (4) and (2) can be conducted using known procedures for reacting pyrrolidines with halogenated compounds. The reaction is typically conducted in an organic solvent at a temperature in the range of from about 20 to 120° C., more typically in the range of about from about 20 to 80° C. Suitable organic solvents include acetonitrile, dimethylsulfoxide, N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMA), ether, and acetone.

Examples of compound (4) include: (R)-2-cyclopentyl-1-(4-dimethylamino-piperidin-1-yl)-2-hydroxy-2-phenylethanone; 2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-thiophen-2-ylethanone; 1-(4-dimethylamino-piperidin-1-yl)-2-hydroxy-4-methyl-2-phenylpentan-1-one; (4-dimethylaminopiperidin-1-yl)(9H-xanthen-9-yl)-methanone; 1-(4-dimethylamino-piperidin-1-yl)-2-hydroxy-2,2-di-thiophen-2-ylethanone; 2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-phenylethanone; and 2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-p-tolylethanone.

Compound (4) may be formed by a coupling reaction of compound (1′) and (4a) under conventional amide bond-forming conditions:

Suitable carboxylic acid/amine coupling reagents include benzotriazol-1-yloxytris-(dimethylamino)phosphonium hexafluorophosphate (BOP), benzotriazol-1-yloxy-tripyrrolidinophosphonium hexafluorophosphate (PyBOP), O-(7-azabenzotriazol-1-yl-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU), 1-hydroxybenzotriazole hydrate (HOBt), dicyclohexylcarbodiimide (DCC), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDCI), carbonyldiimidazole (CDI), and the like. Coupling reactions are conducted in an inert solvent such as DCM in the presence of one or more coupling reagents and a base such as DIPEA, and are performed under conventional amide bond-forming conditions. Note that a coupling reagent may not be required. For example, compounds (1′) and (4a) can be coupled using DMF as the solvent and DIPEA as the base.

Alternately, compound (4), where R³ is —OH, may be formed by a coupling reaction of compound (4a) and (4b), under conventional amide bond-forming conditions, followed by reaction with R³—MgBr:

Examples of compound (4b) include 2-thiopheneglyoxylic acid, benzoylformic acid, and 4-methylphenyl)(oxo)acetic acid. Examples of R³—MgBr include cyclopentyl magnesium bromide, thiophen-2-yl magnesium bromide and isobutyl magnesium bromide.

Process (c)

In process (c), the reaction conditions between compound (4), (5) and (6) will vary depending upon the respective A and B groups. The leaving group represented by L³ can be, for example, a halo, typically bromo. Compound (5) and (6) are generally known or can be prepared from readily available starting materials using well-known synthetic methods.

Some reactions in process (c) are coupling reactions, for example, when Z is —NR^(Z1)C(O)—. In those reactions, the acidic moiety-containing compound may be in the form of a reactive derivative. For example, the carboxylic acid may be activated, for example, by forming an anhydride or carboxylic acid halide, such as a carboxylic acid chloride. Thus the carboxylic acid chloride is a reactive derivative of carboxylic acid. Alternatively, the carboxylic acid can be activated using conventional carboxylic acid/amine coupling reagents, such carbodiimides, O-(7-azabenzotriazol-1-yl-N,N,N′,N′ tetramethyluronium hexafluorophosphate (HATU) and the like. The sulfonic acid and thio acid moieties can be similarly derivatized. The reactions are conducted under conventional conditions using suitable coupling agents such as carbonyldiimidazole. The reaction is typically conducted in the presence of solvents such as trifluoroacetic acid and dichloromethane, and conveniently conducted at a temperature in the range of from −10° C. to 100° C.

The remaining reactions in process (c) are alkylation reactions, for example, when Z is —O—. The reactions are conducted under conventional conditions using suitable solvents such as DMF or DMA, and conveniently conducted at a temperature in the range of from room temperature to 100° C. In addition, process (c) illustrates formation compounds of formula I where the R^(Z2) and/or R^(Z3) moieties are hydrogen. Such compounds are readily converted to compound (1) where R^(Z2) and/or R^(Z3) are —C₁₋₄alkyl or —C₃₋₆cycloalkyl, or are taken together to form an —C₂₋₄alkylene- or —C₂₋₃alkenylene-linkage.

Further details regarding specific reaction conditions and other procedures for preparing representative compounds of the invention or intermediates thereof are described in the Examples set forth below.

Pharmaceutical Compositions and Formulations

Compounds of the invention are typically administered to a patient in the form of a pharmaceutical composition or formulation. Such pharmaceutical compositions may be administered to the patient by any acceptable route of administration including, but not limited to, inhaled, oral, nasal, topical (including transdermal) and parenteral modes of administration. Further, the compounds of the invention may be administered, for example orally, in multiple doses per day, in a single daily dose or a single weekly dose. It will be understood that any form of the compounds of the invention, (i.e., free base, pharmaceutically acceptable salt, solvate, etc.) that is suitable for the particular mode of administration can be used in the pharmaceutical compositions discussed herein.

Accordingly, in one embodiment, the invention is directed to a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a compound of the invention. The compositions may contain other therapeutic and/or formulating agents if desired. A “compound of the invention” may also be referred to herein as the “active agent.”

The pharmaceutical compositions of this invention typically contain a therapeutically effective amount of a compound of the invention. Those skilled in the art will recognize, however, that a pharmaceutical composition may contain more than a therapeutically effective amount, i.e., bulk compositions, or less than a therapeutically effective amount, i.e., individual unit doses designed for multiple administration to achieve a therapeutically effective amount. In one embodiment, the composition will contain from about 0.01-95 wt % of active agent, including, from about 0.01-30 wt %, such as from about 0.01-10 wt %, with the actual amount depending upon the formulation itself, the route of administration, the frequency of dosing, and so forth. In another embodiment, a composition suitable for inhalation, for example, comprises from about 0.01-30 wt % or active agent with yet another embodiment comprises from about 0.01-10 wt % active agent.

Any conventional carrier or excipient may be used in the pharmaceutical compositions of the invention. The choice of a particular carrier or excipient, or combinations of carriers or excipients, will depend on the mode of administration being used to treat a particular patient or type of medical condition or disease state. In this regard, the preparation of a suitable composition for a particular mode of administration is well within the scope of those skilled in the pharmaceutical arts. Additionally, carriers or excipients used in such compositions are commercially available. By way of further illustration, conventional formulation techniques are described in Remington: The Science and Practice of Pharmacy, 20^(th) Edition, Lippincott Williams & White, Baltimore, Md. (2000); and H. C. Ansel et al., Pharmaceutical Dosage Forms and Drug Delivery Systems, 7^(th) Edition, Lippincott Williams & White, Baltimore, Md. (1999).

Representative examples of materials which can serve as pharmaceutically acceptable carriers include, but are not limited to, the following: sugars, such as lactose, glucose and sucrose; starches, such as corn starch and potato starch; cellulose, such as microcrystalline cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients, such as cocoa butter and suppository waxes; oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; glycols, such as propylene glycol; polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; esters, such as ethyl oleate and ethyl laurate; agar; buffering agents, such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer's solution; ethyl alcohol; phosphate buffer solutions; compressed propellant gases, such as chlorofluorocarbons and hydrofluorocarbons; and other non-toxic compatible substances employed in pharmaceutical compositions.

Pharmaceutical compositions are typically prepared by thoroughly and intimately mixing or blending the active agent with a pharmaceutically acceptable carrier and one or more optional ingredients. The resulting uniformly blended mixture may then be shaped or loaded into tablets, capsules, pills, canisters, cartridges, dispensers and the like using conventional procedures and equipment.

In one embodiment, the pharmaceutical compositions are suitable for inhaled administration. Suitable compositions for inhaled administration will typically be in the form of an aerosol or a powder. Such compositions are generally administered using well-known delivery devices, such as a nebulizer inhaler, a dry powder inhaler, or a metered-dose inhaler, examples of which are described below.

In a specific embodiment of the invention, a composition comprising the active agent is administered by inhalation using a nebulizer inhaler. Such nebulizer devices typically produce a stream of high velocity air that causes the composition to spray as a mist that is carried into a patient's respiratory tract. Accordingly, when formulated for use in a nebulizer inhaler, the active agent is typically dissolved in a suitable carrier to form a solution. Alternatively, the active agent can be micronized and combined with a suitable carrier to form a suspension of micronized particles of respirable size, where micronized is typically defined as having particles in which at least about 90 percent of the particles have a mass median diameter of less than about 10 μm. The term “mass median diameter” means the diameter such that half the mass of the particles is contained in particles with larger diameter and half is contained in particles with smaller diameter.

Suitable nebulizer devices include the Respimat® Soft Mist™ Inhaler (Boehringer Ingelheim), the AERx® Pulmonary Delivery System (Aradigm Corp.), and the PARI LC Plus Reusable Nebulizer (Pari GmbH). An exemplary composition for use in a nebulizer inhaler comprises an isotonic aqueous solution comprising from about 0.05 μg/mL to about 10 mg/mL of a compound of the invention. In one embodiment, such a solution has a pH of about 4-6.

In another specific embodiment of the invention, a composition comprising the active agent is administered by inhalation using a dry powder inhaler (DPI). Such DPIs typically administer the active agent as a free-flowing powder that is dispersed in a patient's air-stream during inspiration. In order to achieve a free flowing powder, the active agent is typically formulated with a suitable excipient such as lactose, starch, mannitol, dextrose, polylactic acid, polylactide-co-glycolide, and combinations thereof. Typically, the active agent is micronized and combined with an excipient to form a blend suitable for inhalation. Accordingly, in one embodiment of the invention, the active agent is in micronized form. For example, a representative composition for use in a DPI comprises dry lactose having a particle size between about 1 μm and about 100 μm (e.g., dry milled lactose) and micronized particles of the active agent. Such a dry powder formulation can be made, for example, by combining lactose with the active agent and then dry blending the components. Alternatively, if desired, the active agent can be formulated without an excipient. The composition is then typically loaded into a DPI, or into inhalation cartridges or capsules for use with a DPI. DPIs are well known to those of ordinary skill in the art, and many such devices are commercially available, with representative devices including Aerolizer® (Novartis), Airmax™ (IVAX), ClickHaler® (Innovata Biomed), Diskhaler® (GlaxoSmithKline), Diskus® or Accuhaler (GlaxoSmithKline), Easyhaler® (Orion Pharma), Eclipse™ (Aventis), FlowCaps® (Hovione), Handihaler® (Boehringer Ingelheim), Pulvinal® (Chiesi), Rotahaler® (GlaxoSmithKline), SkyeHaler™ or Certihaler™ (SkyePharma), Twisthaler (Schering-Plough), Turbuhaler® (AstraZeneca), Ultrahaler® (Aventis), and the like.

In yet another specific embodiment of the invention, the composition comprising the active agent is administered by inhalation using a metered-dose inhaler (MDI). Such MDIs typically discharge a measured amount of the active agent using compressed propellant gas. Metered-dose formulations thus typically comprise a solution or suspension of the active agent in a liquefied propellant, such as a chlorofluorocarbon such as CCl₃F or a hydrofluoroalkane (HFA) such as 1,1,1,2-tetrafluoroethane (HFA 134a) and 1,1,1,2,3,3,3-heptafluoro-n-propane (HFA 227), although HFAs are generally preferred due to concerns about chlorofluorocarbons affecting the ozone layer. Additional optional components of HFA formulations include co-solvents, such as ethanol or pentane, and surfactants, such as sorbitan trioleate, oleic acid, lecithin, and glycerin. See, for example, U.S. Pat. No. 5,225,183 to Purewal et al., EP 0717987 A2 (Minnesota Mining and Manufacturing Company), and WO 92/22286 (Minnesota Mining and Manufacturing Company). A representative composition for use in an MDI comprises from about 0.01-5 wt % of active agent; from about 0-20 wt % ethanol; and from about 0-5 wt % surfactant; with the remainder being an HFA propellant. Such compositions are typically prepared by adding a chilled or pressurized hydrofluoroalkane to a suitable container containing the active agent, ethanol (if present) and the surfactant (if present). To prepare a suspension, the active agent is micronized and then combined with the propellant. The formulation is then loaded into an aerosol canister, which forms a portion of the MDI. MDIs are well known to those of ordinary skill in the art, and many such devices are commercially available, with representative devices including AeroBid Inhaler System (Forest Pharmaceuticals), Atrovent Inhalation Aerosol (Boehringer Ingelheim), Flovent® (GlaxoSmithKline), Maxair Inhaler (3M), Proventil® Inhaler (Schering), Serevent® Inhalation Aerosol (GlaxoSmithKline), and the like. Alternatively, a suspension formulation can be prepared by spray drying a coating of surfactant on micronized particles of the active agent. See, for example, WO 99/53901 (Glaxo Group Ltd.) and WO 00/61108 (Glaxo Group Ltd.). Additional examples of processes of preparing respirable particles, and formulations and devices suitable for inhalation dosing are described in U.S. Pat. No. 5,874,063 to Briggner et al.; U.S. Pat. No. 5,983,956 to Trofast; U.S. Pat. No. 6,221,398 to Jakupovic et al.; U.S. Pat. No. 6,268,533 to Gao et al.; U.S. Pat. No. 6,475,524 to Bisrat et al.; and U.S. Pat. No. 6,613,307 to Cooper.

In another embodiment, the pharmaceutical compositions are suitable for oral administration. Suitable compositions for oral administration may be in the form of capsules, tablets, pills, lozenges, cachets, dragees, powders, granules; solutions or suspensions in an aqueous or non-aqueous liquid; oil-in-water or water-in-oil liquid emulsions; elixirs or syrups; and the like; each containing a predetermined amount of the active agent.

When intended for oral administration in a solid dosage form (i.e., as capsules, tablets, pills and the like), the composition will typically comprise the active agent and one or more pharmaceutically acceptable carriers, such as sodium citrate or dicalcium phosphate. Solid dosage forms may also comprise: fillers or extenders, such as starches, microcrystalline cellulose, lactose, sucrose, glucose, mannitol, and/or silicic acid; binders, such as carboxymethylcellulose, alginates, gelatin, polyvinyl pyrrolidone, sucrose and/or acacia; humectants, such as glycerol; disintegrating agents, such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and/or sodium carbonate; solution retarding agents, such as paraffin; absorption accelerators, such as quaternary ammonium compounds; wetting agents, such as cetyl alcohol and/or glycerol monostearate; absorbents, such as kaolin and/or bentonite clay; lubricants, such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and/or mixtures thereof; coloring agents; and buffering agents.

Release agents, wetting agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants may also be present in the pharmaceutical compositions. Exemplary coating agents for tablets, capsules, pills and like, include those used for enteric coatings, such as cellulose acetate phthalate, polyvinyl acetate phthalate, hydroxypropyl methylcellulose phthalate, methacrylic acid-methacrylic acid ester copolymers, cellulose acetate trimellitate, carboxymethyl ethyl cellulose, hydroxypropyl methyl cellulose acetate succinate, and the like. Examples of pharmaceutically acceptable antioxidants include: water-soluble antioxidants, such as ascorbic acid, cysteine hydrochloride, sodium bisulfate, sodium metabisulfate sodium sulfite and the like; oil-soluble antioxidants, such as ascorbyl palmitate, butylated hydroxyanisole, butylated hydroxytoluene, lecithin, propyl gallate, alpha-tocopherol, and the like; and metal-chelating agents, such as citric acid, ethylenediamine tetraacetic acid, sorbitol, tartaric acid, phosphoric acid, and the like.

Compositions may also be formulated to provide slow or controlled release of the active agent using, by way of example, hydroxypropyl methyl cellulose in varying proportions or other polymer matrices, liposomes and/or microspheres. In addition, the pharmaceutical compositions of the invention may contain opacifying agents and may be formulated so that they release the active agent only, or preferentially, in a certain portion of the gastrointestinal tract, optionally, in a delayed manner. Examples of embedding compositions which can be used include polymeric substances and waxes. The active agent can also be in micro-encapsulated form, if appropriate, with one or more of the above-described excipients.

Suitable liquid dosage forms for oral administration include, by way of illustration, pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. Liquid dosage forms typically comprise the active agent and an inert diluent, such as, for example, water or other solvents, solubilizing agents and emulsifiers, such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, oils (e.g., cottonseed, groundnut, corn, germ, olive, castor and sesame oils), glycerol, tetrahydrofuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof. Suspensions may contain suspending agents such as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminium metahydroxide, bentonite, agar-agar and tragacanth, and mixtures thereof.

When intended for oral administration, the pharmaceutical compositions of the invention may be packaged in a unit dosage form. The term “unit dosage form” refers to a physically discrete unit suitable for dosing a patient, i.e., each unit containing a predetermined quantity of the active agent calculated to produce the desired therapeutic effect either alone or in combination with one or more additional units. For example, such unit dosage forms may be capsules, tablets, pills, and the like.

Compounds of the invention can also be administered parenterally (e.g., by subcutaneous, intravenous, intramuscular, or intraperitoneal injection). For such administration, the active agent is provided in a sterile solution, suspension, or emulsion. Exemplary solvents for preparing such formulations include water, saline, low molecular weight alcohols such as propylene glycol, polyethylene glycol, oils, gelatin, fatty acid esters such as ethyl oleate, and the like. A typical parenteral formulation is a sterile pH 4-7 aqueous solution of the active agent. Parenteral formulations may also contain one or more solubilizers, stabilizers, preservatives, wetting agents, emulsifiers, and dispersing agents. These formulations may be rendered sterile by use of a sterile injectable medium, a sterilizing agent, filtration, irradiation, or heat.

Compounds of the invention can also be administered transdermally using known transdermal delivery systems and excipients. For example, the compound can be admixed with permeation enhancers, such as propylene glycol, polyethylene glycol monolaurate, azacycloalkan-2-ones and the like, and incorporated into a patch or similar delivery system. Additional excipients including gelling agents, emulsifiers and buffers, may be used in such transdermal compositions if desired.

If desired, the compounds of this invention may be administered in combination with one or more other therapeutic agents. Thus, in one embodiment, compositions of the invention may optionally contain other drugs that are co-administered with a compound of the invention. For example, the composition may further comprise one or more drugs (also referred to as “secondary agents(s)”) selected from the group of other bronchodilators (e.g., PDE₃ inhibitors, adenosine 2b modulators and β₂ adrenergic receptor agonists); anti-inflammatory agents (e.g., steroidal anti-inflammatory agents such as corticosteroids and glucocorticoids; non-steroidal anti-inflammatory agents (NSAIDs); and PDE₄ inhibitors); other muscarinic receptor antagonists (i.e., antichlolinergic agents); antiinfective agents (e.g., Gram positive and Gram negative antibiotics, and antiviral agents); antihistamines; protease inhibitors; afferent blockers (e.g., D₂ agonists and neurokinin modulators); and combinations thereof. Numerous examples of such therapeutic agents are well known in the art, and examples are described below. By combining a compound of the invention with a secondary agent, double therapy can be achieved, i.e., muscarinic receptor antagonist activity and activity associated with the secondary agent (e.g., β₁ adrenergic receptor agonist), in some cases by administering two compositions and in some cases by administering a single composition containing the active agent and the secondary agent. Accordingly, in yet another aspect of the invention, a pharmaceutical composition comprises a compound of the invention, a second active agent, and a pharmaceutically acceptable carrier. Third, fourth etc. active agents may also be included in the composition. For example, a composition may comprise a compound of the invention; a secondary agent selected from corticosteroids, β₂ adrenergic receptor agonists; phosphodiesterase-4 inhibitors, and combinations thereof; and a pharmaceutically acceptable carrier. In a specific embodiment, the composition comprises a compound of the invention, a β₂ adrenergic receptor agonist, and a steroidal anti-inflammatory agent. In combination therapy, the amount of compound of the invention that is administered, as well as the amount of secondary agents, may be less than the amount typically administered in monotherapy.

A compound of the invention may be either physically mixed with the second active agent to form a composition containing both agents; or each agent may be present in separate and distinct compositions which are administered to the patient simultaneously or sequentially. For example, a compound of the invention can be combined with a second active agent using conventional procedures and equipment to form a combination of active agents comprising a compound of the invention and a second active agent. Additionally, the active agents may be combined with a pharmaceutically acceptable carrier to form a pharmaceutical composition comprising a compound of the invention, a second active agent and a pharmaceutically acceptable carrier. In this embodiment, the components of the composition are typically mixed or blended to create a physical mixture. The physical mixture is then administered in a therapeutically effective amount using any of the routes described herein.

Alternatively, the active agents may remain separate and distinct before administration to the patient. In this embodiment, the agents are not physically mixed together before administration but are administered simultaneously or at separate times as separate compositions. Such compositions can be packaged separately or may be packaged together in a kit. When administered at separate times, the secondary agent will typically be administered less than 24 hours after administration of the compound of the invention. In other embodiments this timed relationship is less than 12 hours, less than 8 hours, less than 6 hours, less than 4 hours, less than 3 hours, less than 1 hour, less than thirty minutes, less than ten minutes, less than one minute, or immediately after administration of the compound of the invention. This is also referred to as sequential administration. Thus, a compound of the invention can be administered by inhalation simultaneously or sequentially with another active agent using an inhalation delivery device that employs separate compartments (e.g. blister packs) for each active agent, where sequential may mean being administered immediately after administration of the compound of the invention or at some predetermined time later (e.g., one hour later or three hours later). Alternatively, the combination may be administered using separate delivery devices, i.e., one delivery device for each agent. Additionally, the agents can be delivered by different routes of administration, i.e., one by inhalation and the other by oral administration.

In one embodiment, the kit comprises a first dosage form comprising a compound of the invention and at least one additional dosage form comprising one or more of the secondary agents set forth herein, in quantities sufficient to carry out the methods of the invention. The first dosage form and the second (or third, etc,) dosage form together comprise a therapeutically effective amount of active agents for the treatment or prevention of a disease or medical condition in a patient.

Secondary agent(s), when included, are present in a therapeutically effective amount. i.e., are typically administered in an amount that produces a therapeutically beneficial effect when co-administered with a compound of the invention. The secondary agent can be in the form of a pharmaceutically acceptable salt, solvate, optically pure stereoisomer, and so forth. Thus, secondary agents listed below are intended to include all such forms, and are commercially available or can be prepared using conventional procedures and reagents. Suitable doses for a secondary agent are typically in the range of about 0.05 μg/day to about 500 mg/day.

In a particular embodiment, a compound of the invention is administered in combination with a β₂ adrenergic receptor agonist. Representative β₂ adrenergic receptor agonists include, but are not limited to, albuterol, bitolterol, fenoterol, formoterol, indacaterol, isoetharine, levalbuterol, metaproterenol, pirbuterol, salbutamol, salmefamol, salmeterol, terbutaline, and the like. Other β₂ adrenergic receptor agonists that can be used in combination with compounds of the invention include, but are not limited to, 3-(4-{[6-({(2R)-2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl}amino)hexyl]oxy}butyl)-benzenesulfonamide and 3-(-3-{[7-({(2R)-2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)-phenyl]ethyl}amino)heptyl]oxy}propyl)benzenesulfonamide and related compounds disclosed in WO 02/066422 (Glaxo Group Ltd.); 3-[3-(4-{[6-([(2R)-2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl}amino)hexyl]oxy}butyl)-phenyl]imidazolidine-2,4-dione and related compounds disclosed in WO 02/070490 (Glaxo Group Ltd.); 3-(4-{[6-({(2R)-2-[3-(formylamino)-4-hydroxyphenyl]-2-hydroxyethyl}amino)hexyl]oxy}-butyl)benzenesulfonamide, 3-(4-{[6-({(2S)-2-[3-(formylamino)-4-hydroxyphenyl]-2-hydroxyethyl}amino)hexyl]oxy}butyl)-benzenesulfonamide, 3-(4-{[6-({(2R/S)-2-[3-(formylamino)-4-hydroxyphenyl]-2-hydroxyethyl}amino)hexyl]oxy}butyl)benzene-sulfonamide, N-(t-butyl)-3-(4-{[6-({(2R)-2-[3-(formylamino)-4-hydroxyphenyl]-2-hydroxyethyl}amino)hexyl]-oxy}butyl)benzenesulfonamide, N-(tert-butyl)-3-(4-{[6-({(2S)-2-[3-(formylamino)-4-hydroxyphenyl]-2-hydroxyethyl}amino)hexyl]oxy}butyl)-benzenesulfonamide, N-(t-butyl)-3-(4-{[6-({(2R/S)-2-[3-(formylamino)-4-hydroxyphenyl]-2-hydroxyethyl}amino)hexyl]-oxy}butyl)benzenesulfonamide and related compounds disclosed in WO 02/076933 (Glaxo Group Ltd.); 4-{(1R)-2-[(6-{2-[(2,6-dichlorobenzyl)-oxy]ethoxy}hexyl)amino]-1-hydroxyethyl}-2-(hydroxymethyl)phenol and related compounds disclosed in WO 03/024439 (Glaxo Group Ltd.); N-{2-[4-((R)-2-hydroxy-2-phenylethylamino)phenyl]ethyl}-(R)-2-hydroxy-2-(3-formamido-4-hydroxyphenyl)-ethylamine and related compounds disclosed in U.S. Pat. No. 6,576,793 to Moran et al.; N-{2-[4-(3-phenyl-4-methoxyphenyl)aminophenyl]ethyl}-(R)-2-hydroxy-2-(8-hydroxy-2(1H)-quinolinon-5-yl)ethylamine and related compounds disclosed in U.S. Pat. No. 6,653,323 to Moran et al. In a particular embodiment, the β₂-adrenoreceptor agonist is a crystalline monohydrochloride salt of N-{2-[4-((R)-2-hydroxy-2-phenylethylamino)-phenyl]ethyl}-(R)-2-hydroxy-2-(3-formamido-4-hydroxyphenyl)ethylamine. Typically, the β₂-adrenoreceptor agonist will be administered in an amount sufficient to provide from about 0.05-500 μg per dose.

In a particular embodiment, a compound of the invention is administered in combination with a steroidal anti-inflammatory agent. Representative steroidal anti-inflammatory agents include, but are not limited to, beclomethasone dipropionate; budesonide; butixocort propionate; 20R-16α,17α-[butylidenebis(oxy)]-6α,9α-difluoro-11β-hydroxy-17β-(methylthio)androsta-4-en-3-one (RPR-106541); ciclesonide; dexamethasone; 6α,9α-difluoro-17α-[(2-furanylcarbonyl)oxy]-11β-hydroxy-16α-methyl-3-oxoandrosta-1,4-diene-17β-carbothioic acid S-fluoromethyl ester; 6α,9α-difluoro-11β-hydroxy-16α-methyl-17α-[(4-methyl-1,3-thiazole-5-carbonyl)oxy]-3-oxoandrosta-1,4-diene-17β-carbothioic acid S-fluoromethyl ester; 6α,9α-difluoro-11β-hydroxy-16α-methyl-3-oxo-17α-propionyloxyandrosta-1,4-diene-17β-carbothioic acid (S)-(2-oxotetra-hydrofuran-3S-yl) ester; flunisolide; fluticasone propionate; methyl prednisolone; mometasone furoate; prednisolone; prednisone; rofleponide; ST-126; triamcinolone acetonide; and the like. Typically, the steroidal anti-inflammatory agent will be administered in an amount sufficient to provide from about 0.05-500 μg per dose.

An exemplary combination is a compound of the invention co-administered with salmeterol as the β₂ adrenergic receptor agonist, and fluticasone propionate as the steroidal anti-inflammatory agent. Another exemplary combination is a compound of the invention co-administered with a crystalline monohydrochloride salt of N-{2-[4-((R)-2-hydroxy-2-phenylethylamino)phenyl]ethyl}-(R)-2-hydroxy-2-(3-formamido-4-hydroxyphenyl)-ethylamine as the β₂-adrenoreceptor agonist, and 6α,9α-difluoro-17α-[(2-furanylcarbonyl)-oxy]-11β-hydroxy-16α-methyl-3-oxoandrosta-1,4-diene-17β-carbothioic acid S-fluoromethyl ester as the steroidal anti-inflammatory agent.

Other suitable combinations include, for example, other anti-inflammatory agents, e.g., NSAIDs (such as sodium cromoglycate; nedocromil sodium; phosphodiesterase (PDE) inhibitors (e.g., theophylline, PDE4 inhibitors or mixed PDE3/PDE4 inhibitors); leukotriene antagonists (e.g., monteleukast); inhibitors of leukotriene synthesis; iNOS inhibitors; protease inhibitors, such as tryptase and elastase inhibitors; beta-2 integrin antagonists and adenosine receptor agonists or antagonists (e.g., adenosine 2a agonists); cytokine antagonists (e.g., chemokine antagonists such as, an interleukin antibody (αIL antibody), specifically, an αIL-4 therapy, an αIL-13 therapy, or a combination thereof); or inhibitors of cytokine synthesis.

In a particular embodiment, a compound of the invention is administered in combination with a phosphodiesterase-4 (PDE4) inhibitors or mixed PDE3/PDE4 inhibitors. Representative PDE4 or mixed PDE3/PDE4 inhibitors include, but are not limited to, cis 4-cyano-4-(3-cyclopentyloxy-4-methoxyphenyl)cyclohexan-1-carboxylic acid, 2-carbomethoxy-4-cyano-4-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)-cyclohexan-1-one; cis-[4-cyano-4-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)-cyclohexan-1-ol]; cis-4-cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]cyclohexane-1-carboxylic acid and the like, or pharmaceutically acceptable salts thereof. Other representative PDE4 or mixed PDE4/PDE3 inhibitors include AWD-12-281 (elbion); NCS-613 (INSERM); D-4418 (Chiroscience and Schering-Plough); CI-1018 or PD-168787 (Pfizer); benzodioxole compounds disclosed in WO99/16766 (Kyowa Hakko); K-34 (Kyowa Hakko); V-11294A (Napp); roflumilast (Byk-Gulden); pthalazinone compounds disclosed in WO99/47505 (Byk-Gulden); Pumafentrine (Byk-Gulden, now Altana); arofylline (Almirall-Prodesfarma); VM554/UM565 (Vernalis); T-440 (Tanabe Seiyaku); and T2585 (Tanabe Seiyaku).

In a particular embodiment, a compound of the invention is administered in combination with a muscarinic antagonist (i.e., anticholinergic agent). Representative muscarinic antagonists include, but are not limited to, atropine, atropine sulfate, atropine oxide, methylatropine nitrate, homatropine hydrobromide, hyoscyamine (d, l) hydrobromide, scopolamine hydrobromide, ipratropium bromide, oxitropium bromide, tiotropium bromide, methantheline, propantheline bromide, anisotropine methyl bromide, clidinium bromide, copyrrolate (Robinul), isopropamide iodide, mepenzolate bromide, tridihexethyl chloride (Pathilone), hexocyclium methylsulfate, cyclopentolate hydrochloride, tropicamide, trihexyphenidyl hydrochloride, pirenzepine, telenzepine, AF-DX 116 and methoctramine and the like.

In a particular embodiment, a compound of the invention is administered in combination with an antihistamine (i.e., H₁-receptor antagonist). Representative antihistamines include, but are not limited to, ethanolamines, such as carbinoxamine maleate, clemastine fumarate, diphenylhydramine hydrochloride and dimenhydrinate; ethylenediamines, such as pyrilamine amleate, tripelennamine hydrochloride and tripelennamine citrate; alkylamines, such as chlorpheniramine and acrivastine; piperazines, such as hydroxyzine hydrochloride, hydroxyzine pamoate, cyclizine hydrochloride, cyclizine lactate, meclizine hydrochloride and cetirizine hydrochloride; piperidines, such as astemizole, levocabastine hydrochloride, loratadine or its descarboethoxy analogue, terfenadine and fexofenadine hydrochloride; azelastine hydrochloride; and the like.

The following formulations illustrate representative pharmaceutical compositions of the invention.

Exemplary Compositions for Administration by a DPI

A compound of the invention (0.2 mg) is micronized and then blended with lactose (25 mg). This blended mixture is then loaded into a gelatin inhalation cartridge. The contents of the cartridge are administered using a DPI, for example.

A micronized compound of the invention (100 mg) is blended with milled lactose (25 g) (e.g., lactose in which not greater than about 85% of the particles have a MMD of about 60 μm to about 90 μm and not less than 15% of the particles have a MMD of less then 15 μm). This blended mixture is then loaded into individual blisters of a peelable blister pack in an amount sufficient to provide about 10 μg to about 500 μg of the compound of the invention per dose. The contents of the blisters are administered using a DPI.

A micronized compound of the invention (1 g) is blended with milled lactose (200 g) to form a bulk composition having a weight ratio of compound to milled lactose of 1:200. The blended composition is packed into a DPI capable of delivering between about 10 μg to about 500 μg of the compound of the invention per dose.

A micronized compound of the invention (100 mg) and a micronized β₂ adrenergic receptor agonist (500 mg) are blended with milled lactose (30 g). The blended mixture is then loaded into individual blisters of a peelable blister pack in an amount sufficient to provide about 10 μg to about 500 μg of the compound of the invention per dose. The contents of the blisters are administered using a DPI.

Exemplary Compositions for Use in an MDI

A micronized compound of the invention (10 g) is dispersed in a solution prepared by dissolving lecithin (0.2 g) in demineralized water (200 mL). The resulting suspension is spray dried and then micronized to form a micronized composition comprising particles having a mean diameter less than about 1.5 μm. The micronized composition is then loaded into MDI cartridges containing pressurized 1,1,1,2-tetrafluoroethane in an amount sufficient to provide about 10 μg to about 500 μg of the compound of the invention per dose when administered by the MDI.

A suspension containing 5 wt % compound of the invention, 0.5 wt % lecithin, and 0.5 wt % trehalose is prepared by dispersing 5 g of a compound of the invention as micronized particles with mean size less than 10 μm in a colloidal solution formed from 0.5 g of trehalose and 0.5 g of lecithin dissolved in 100 mL of demineralized water. The suspension is spray dried and the resulting material is micronized to particles having a mean diameter less than 1.5 μm. The particles are loaded into canisters with pressurized 1,1,1,2-tetrafluoroethane.

Exemplary Composition for Use in a Nebulizer Inhaler

A compound of the invention (25 mg) is dissolved in citrate buffered (pH 5) isotonic saline (125 mL). The mixture is stirred and sonicated until the compound is dissolved. The pH of the solution is checked and adjusted, if necessary, to pH 5 by slowly adding aqueous 1N NaOH. The solution is administered using a nebulizer device that provides about 10 μg to about 500 μg of the compound of the invention per dose.

Exemplary Hard Gelatin Capsules for Oral Administration

A compound of the invention (50 g), spray-dried lactose (440 g) and magnesium stearate (10 g) are thoroughly blended. The resulting composition is then loaded into hard gelatin capsules (500 mg of composition per capsule).

Exemplary Suspension for Oral Administration

The following ingredients are mixed to form a suspension containing 100 mg of compound per 10 mL of suspension:

Ingredients Amount Compound of the invention 1.0 g Fumaric acid 0.5 g Sodium chloride 2.0 g Methyl paraben 0.15 g Propyl paraben 0.05 g Granulated sugar 25.5 g Sorbitol (70% solution) 12.85 g Veegum ® K (magnesium aluminum silicate) 1.0 g Flavoring 0.035 mL Colorings 0.5 mg Distilled water q.s. to 100 mL

Exemplary Injectable Formulation for Administration by Injection

compound of the invention (0.2 g) is blended with 0.4 M sodium acetate buffer solution (2.0 mL). The pH is then adjusted to pH 4 using 0.5 N aqueous hydrochloric acid or 0.5 N aqueous sodium hydroxide, as necessary, and then sufficient water for injection is added to provide a total volume of 20 mL. The mixture is then filtered through a sterile filter (0.22 micron) to provide a sterile solution suitable for administration by injection.

Utility

Compounds of the invention possess muscarinic receptor antagonist activity, and in one embodiment, at nanomolar potencies. In one embodiment, compounds of the invention are selective for inhibition of M₃ muscarinic receptor subtype activity over M₂ muscarinic receptor subtype activity. In another embodiment, compounds of the invention are selective for inhibition of M₃ and M₂ muscarinic receptor subtype activity over M₁, M₄, and M₅ muscarinic receptor subtype activity. Additionally, compounds of the invention are expected to possess a desirable duration of action. Accordingly, in another specific embodiment, the invention is directed to compounds having a duration of action greater than about 24 hours. Moreover, compounds of the invention are also expected to possess reduced side effects, such as dry mouth, at efficacious doses when administered by inhalation compared to other known muscarinic receptor antagonists administered by inhalation (such as tiotropium).

One measure of the affinity of a compound for the M₃ receptor subtype is the inhibition dissociation constant (K_(i)) for binding to the receptor. Compounds of the invention are expected to have a K_(i) for the M₃ receptor subtype of less than or equal to 100 nM, as determined, for example, by an in vitro radioligand displacement assay. Compounds of particular interest include those having a K_(i) less than or equal to 50 nM, and in another embodiment, the compounds have a K_(i) less than or equal to 10 nM, and in yet another embodiment, the compounds have a K_(i) less than or equal to 1.0 nM. Compounds of even more particular interest include those having a K_(i) less than or equal to 500 pM, and in another embodiment, the compounds have a K_(i) less than or equal to 200 pM. It is noted that in some cases, compounds of the invention may possess weak muscarinic receptor antagonist activity. In such cases, those of skill in the art will recognize that these compounds still have utility as research tools.

Also of particular interest are those compounds having an ID₅₀ of less than or equal to 100 μg/mL at 24 hours post dosing, more particularly those compounds having an ID₅₀ of less than or equal to 30 μg/mL at 24 hours post dosing.

Exemplary assays to determine properties of compounds of the invention, such as the muscarinic receptor antagonizing activity, are described in the Examples and include by way of illustration and not limitation, assays that measure hM₁, hM₂, hM₃, hM₄, and hM₅ muscarinic receptor binding (for example, as described in Assay 1). Useful functional assays to determine the muscarinic receptor antagonizing activity of compounds of the invention include by way of illustration and not limitation, assays that measure ligand-mediated changes in intracellular cyclic adenosine monophosphate (cAMP), ligand-mediated changes in activity of the enzyme adenylyl cyclase (which synthesizes cAMP), ligand-mediated changes in incorporation of guanosine 5′-O-(γ-thio)triphosphate ([³⁵S]GTPγS) into isolated membranes via receptor catalyzed exchange of [³⁵S]GTPγS for guanosine diphosphate, ligand-mediated changes in free intracellular calcium ions (measured, for example, with a fluorescence-linked imaging plate reader or FLIPR® from Molecular Devices, Inc.), and the like. Exemplary assays are described in Assay 2. Compounds of this invention are expected to antagonize or decrease the activation of muscarinic receptors in any of the assays listed above, or assays of a similar nature, and will typically be used in these studies at a concentration ranging from about 0.1-100 nanomolar. Thus, the aforementioned assays are useful in determining the therapeutic utility, for example, the bronchodilating activity, of compounds of the invention.

Other properties and utilities of compounds of the invention can be demonstrated using various in vitro and in vivo assays well-known to those skilled in the art. For example, the in vivo potency of compounds of the invention can be measured in an animal model such as the Einthoven model. Briefly, the bronchodilator activity of a compound is evaluated in an anesthetized animal (the Einthoven model), which uses ventilation pressure as a surrogate measure of airway resistance. See, for example, Einthoven (1892) Pfugers Arch. 51:367-445; and Mohammed et al. (2000) Pulm Pharmacol Ther. 13(6):287-92, as well as Assay 3 which describes a rat Einthoven model. In one embodiment, a compound of the invention administered at a dose of 100 μg/ml in the rat Einthoven model exhibits greater than or equal to 35% inhibition of the bronchoconstrictor response at 24 hours, and in another embodiment exhibits greater than or equal to 70% inhibition at 24 hours. Another useful in vivo assay is the rat antisialagogue assay (for example, as described in Assay 4).

The quaternary compounds of the invention also provide surprising advantages over the corresponding non-quaternary compounds, as manifested, for example, in improved in vivo potency. For example, the following secondary and tertiary compounds:

exhibit a hM₃ K_(i) value of 0.42 and 0.38 nM measured in a binding assay such as described in Assay 1 (measured at 6 hours), respectively. When evaluated in a rat Einthoven assay such as that described in Assay 3 (100 μg dose; measured at 24 hours), the secondary and tertiary compounds exhibited −6% and −18% inhibition of MCh response relative to control animals, respectively. On the other hand, quaternary compounds of the invention, such as [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin-4-yl][2-(4-hydroxyphenyl)ethyl]dimethylammonium (Example 3-3):

exhibited a hM₃ K_(i) value of 0.74 nM and 76% inhibition, when evaluated under the same or similar conditions.

Compounds of the invention are expected to be useful as therapeutic agents for treating medical conditions mediated by muscarinic receptors. Thus it is expected that patients suffering from a disease or disorder that is treated by blocking the muscarinic receptor can be treated by administering a therapeutically effective amount of a muscarinic receptor antagonist of the invention. Such medical conditions include, by way of example, pulmonary disorders or diseases including those associated with reversible airway obstruction, such as chronic obstructive pulmonary disease (e.g., chronic and wheezy bronchitis and emphysema), asthma, pulmonary fibrosis, allergic rhinitis, rhinorrhea, and the like. Other medical conditions that can be treated with muscarinic receptor antagonists are genitourinary tract disorders, such as overactive bladder or detrusor hyperactivity and their symptoms; gastrointestinal tract disorders, such as irritable bowel syndrome, diverticular disease, achalasia, gastrointestinal hypermotility disorders and diarrhea; cardiac arrhythmias, such as sinus bradycardia; Parkinson's disease; cognitive disorders, such as Alzheimer's disease; dismenorrhea; and the like.

The amount of active agent administered per dose or the total amount administered per day may be predetermined or it may be determined on an individual patient basis by taking into consideration numerous factors, including the nature and severity of the patient's condition, the condition being treated, the age, weight, and general health of the patient, the tolerance of the patient to the active agent, the route of administration, pharmacological considerations such as the activity, efficacy, pharmacokinetics and toxicology profiles of the active agent and any secondary agents being administered, and the like. Treatment of a patient suffering from a disease or medical condition (such as COPD) can begin with a predetermined dosage or a dosage determined by the treating physician, and will continue for a period of time necessary to prevent, ameliorate, suppress, or alleviate the symptoms of the disease or medical condition. Patients undergoing such treatment will typically be monitored on a routine basis to determine the effectiveness of therapy. For example, in treating COPD, significant improvement in forced expiratory volume (measured in one second) may be used to determine the effectiveness of treatment. Similar indicators for the other diseases and conditions described herein, are well-known to those skilled in the art, and are readily available to the treating physician. Continuous monitoring by the physician will insure that the optimal amount of active agent will be administered at any given time, as well as facilitating the determination of the duration of treatment. This is of particular value when secondary agents are also being administered, as their selection, dosage, and duration of therapy may also require adjustment. In this way, the treatment regimen and dosing schedule can be adjusted over the course of therapy so that the lowest amount of active agent that exhibits the desired effectiveness is administered and, further, that administration is continued only so long as is necessary to successfully treat the disease or medical condition.

Accordingly, in one embodiment, compounds of the invention are useful for treating smooth muscle disorders in mammals, including humans and their companion animals (e.g., dogs, cats etc.). Such smooth muscle disorders include, by way of illustration, overactive bladder, chronic obstructive pulmonary disease and irritable bowel syndrome. Typically, suitable doses for treating smooth muscle disorders or other disorders mediated by muscarinic receptors will range from about 0.14 μg/kg/day to about 7 mg/kg/day of active agent; including from about 0.15 μg/kg/day to about 5 mg/kg/day. For an average 70 kg human, this would amount to about 10 μg per day to about 500 mg per day of active agent.

In a specific embodiment, compounds of the invention are useful for treating pulmonary or respiratory disorders, such as COPD or asthma, in mammals including humans, by administering to a patient a therapeutically effective amount of the compound. Generally, the dose for treating a pulmonary disorder will range from about 10-1500 μg/day. The term “COPD” is understood by those of ordinary skill in the art to include a variety of respiratory conditions, including chronic obstructive bronchitis and emphysema, as exemplified by the teachings of Barnes (2000) N. Engl. J. Med. 343:269-78, and references cited therein. When used to treat a pulmonary disorder, compounds of the invention are optionally administered in combination with other therapeutic agents such as a β₂-adrenoreceptor agonist; a corticosteroid, a non-steroidal anti-inflammatory agent, or combinations thereof.

When administered by inhalation, compounds of the invention typically have the effect of producing bronchodilation. Accordingly, in another of its method aspects, the invention is directed to a method of producing bronchodilation in a patient, comprising administering to a patient a bronchodilation-producing amount of a compound of the invention. Generally, the therapeutically effective dose for producing bronchodilation will range from about 10-1500 μg/day.

In another embodiment, compounds of the invention are used to treat overactive bladder. When used to treat overactive bladder, a typical dose will range from about 1.0-500 mg/day. In yet another embodiment, compounds of the invention are used to treat irritable bowel syndrome. When used to treat irritable bowel syndrome, compounds of the invention will typically be administered orally or rectally, and a typical dose will range from about 1.0-500 mg/day.

Since compounds of this invention possess muscarinic receptor antagonist activity, such compounds are also useful as research tools for investigating or studying biological systems or samples having muscarinic receptors. Any suitable biological system or sample having M₁, M₂, M₃, M₄ and/or M₅ muscarinic receptors may be employed in such studies which may be conducted either in vitro or in vivo. Representative biological systems or samples suitable for such studies include, but are not limited to, cells, cellular extracts, plasma membranes, tissue samples, isolated organs, mammals (such as mice, rats, guinea pigs, rabbits, dogs, pigs, humans, and so forth), and the like, with mammals being of particular interest. In one particular embodiment of the invention a muscarinic receptor in a mammal is antagonized by administering a muscarinic receptor-antagonizing amount of a compound of the invention. Compounds of the invention can also be used as research tools by conducting biological assays using such compounds.

When used as a research tool, a biological system or sample comprising a muscarinic receptor is typically contacted with a muscarinic receptor-antagonizing amount of a compound of the invention. After the biological system or sample is exposed to the compound, the effects of antagonizing the muscarinic receptor are determined using conventional procedures and equipment, such as by measuring binding in a radioligand binding assays or ligand-mediated changes in a functional assay or by determining the amount of bronchoprotection provided by the compound in a bronchoprotection assay in a mammal. Exposure encompasses contacting cells or tissue with the compound, administering the compound to a mammal, for example by i.p. or i.v. administration, and so forth. This determining step may comprise measuring a response, i.e., a quantitative analysis or may comprise an observation, i.e., a qualitative analysis. Measuring a response involves, for example, determining the effects of the compound on the biological system or sample using conventional procedures and equipment, such as radioligand binding assays and measuring ligand-mediated changes in functional assays. The assay results can be used to determine the activity level as well as the amount of compound necessary to achieve the desired result, i.e., a muscarinic-antagonizing amount. Typically, the determining step will involve determining the muscarinic receptor ligand-mediated effects.

Additionally, compounds of the invention can be used as research tools for evaluating other chemical compounds, and thus are also useful in screening assays to discover, for example, new compounds having muscarinic receptor binding activity. In this manner, a compound of the invention is used as a standard in an assay to allow comparison of the results obtained with a test compound and with compounds of the invention to identify those test compounds that have about equal or superior binding, if any. For example, muscarinic receptor binding data (as determined, for example, by in vitro radioligand displacement assays) for a test compound or a group of test compounds is compared to the muscarinic receptor binding data for a compound of the invention to identify those test compounds that have the desired properties, e.g., test compounds having binding about equal or superior to a compound of the invention, if any. Alternatively, for example, bronchoprotective effects can be determined for test compounds and a compound of the invention in a bronchoprotection assay in a mammal and this data compared to identify test compounds providing about equal or superior bronchoprotective effects. This aspect of the invention includes, as separate embodiments, both the generation of comparison data (using the appropriate assays) and the analysis of the test data to identify test compounds of interest. Thus, a test compound can be evaluating in a biological assay, by a method comprising the steps of: (a) conducting a biological assay with a test compound to provide a first assay value; (b) conducting the biological assay with a compound of the invention to provide a second assay value; wherein step (a) is conducted either before, after or concurrently with step (b); and (c) comparing the first assay value from step (a) with the second assay value from step (b). Exemplary biological assays include muscarinic receptor binding assays.

EXAMPLES

The following Preparations and Examples are provided to illustrate specific embodiments of the invention. These specific embodiments, however, are not intended to limit the scope of the invention in any way unless specifically indicated.

The following abbreviations have the following meanings unless otherwise indicated and any other abbreviations used herein and not defined have their standard meaning:

BSA bovine serum albumin

cAMP 3′-5′ cyclic adenosine monophosphate

cM₅ cloned chimpanzee M₅ receptor

DCM dichloromethane

DIPEA N,N-diisopropylethylamine

DMA N,N-dimethylacetamide

DMF N,N-dimethylformamide

dPBS Dulbecco's phosphate buffered saline

EDCI 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride

EDTA ethylenediamine tetraacetic acid

EtOAc ethyl acetate

HBSS Hank's Buffered Salt Solution

HEPES 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid

hM₁ cloned human M₁ receptor

hM₂ cloned human M₂ receptor

hM₃ cloned human M₃ receptor

hM₄ cloned human M₄ receptor

hM₅ cloned human M₅ receptor

HOBt 1-hydroxybenzotriazole hydrate

MeOH methanol

THF tetrahydrofuran

Any other abbreviations used herein but not defined have their standard, generally accepted meaning. Unless noted otherwise, all materials, such as reagents, starting materials and solvents, were purchased from commercial suppliers (such as Sigma-Aldrich, Fluka Riedel-de Haën, and the like) and were used without further purification. Reactions were run under nitrogen atmosphere, unless noted otherwise. Progress of reaction mixtures was monitored by thin layer chromatography (TLC), analytical high performance liquid chromatography (anal. HPLC), and mass spectrometry, the details of which are given below and separately in specific examples of reactions. Reaction mixtures were worked up as described specifically in each reaction; commonly they were purified by extraction and other purification methods such as temperature-, and solvent-dependent crystallization, and precipitation. In addition, reaction mixtures were routinely purified by preparative HPLC.

Preparation 1 (R)-Cyclopentylhydroxyphenyl acetic Acid

(2R,5R)-2-t-Butyl-5-phenyl-1,3-dioxolan-4-one (1a): (R)-Mandelic acid (20 g, 130 mmol) was dissolved in anhydrous pentane (200 mL, 1.7 mol). Pivaldehyde (13.6 g, 153 mmol) was added followed by trifluoromethanesulfonic acid (488 μL, 5.4 mmol). The mixture was allowed to reflux at 36° C. under nitrogen. After 5.5 hours, the mixture was allowed to cool to room temperature before stirring with 200 mL of an 8 wt % NaHCO₃ solution for 10 minutes. Excess pentane was removed by rotary evaporation. The solids were collected by filtration and rinsed (100 mL water) while under vacuum filtration. The solids were dried overnight under high vacuum to yield 23.8 grams of intermediate (1a) as a white solid (88% purity).

(2R,5S)-2-t-Butyl-5-(1-hydroxycyclopentyl)-5-phenyl-1,3-dioxolan-4-one (1b): Lithium hexamethyldisilazide (0.8 g, 4.7 mmol; 4.7 mL of 1.0 M in hexanes) was added to anhydrous THF (5.3 mL, 65 mmol) at −78° C. Intermediate (1a) (800 mg, 3.6 mmol) in 5.3 mL anhydrous THF was added to the solution dropwise over 15 minutes. After 30 minutes cyclopentanone (451 μL, 5.1 mmol) was added dropwise over less than 1 minute. After 2 hours, 0.8 mL of saturated aqueous Na₂HPO₄ was added, and the mixture stirred at room temperature for 5 minutes. The mixture was added to 8 mL saturated aqueous ammonium chloride. The aqueous layer was washed (2×80 mL EtOAc), and the organic layers were combined, dried over Na₂SO₄, filtered, and concentrated. The crude product (780 mg) was purified by flash chromatography (5-15% EtOAc gradient over 30 minutes with hexanes) to yield intermediate (1b).

(2R,5S)-2-t-Butyl-5-cyclopent-1-enyl-5-phenyl-1,3-dioxolan-4-one (1c): Intermediate (1b) (650 mg, 2.1 mmol) was dissolved in 6.8 mL anhydrous THF and the solution was cooled to 0° C. Thionyl chloride (436 μL, 6 mmol) was added dropwise, followed by the addition of pyridine (777 μL, 9.6 mmol). The mixture was stirred at 0° C. for 1 hour. Saturated aqueous ammonium chloride (14 mL) was added and the mixture was stirred for 5 minutes while warming to room temperature. The layers were separated, and the aqueous layer was washed (2×100 mL EtOAc.). The organic layers were combined, dried over Na₂SO₄, filtered, and concentrated to yield intermediate (1c) as a light yellow oil (540 mg), which was used in the next step without further purification.

(S)-Cyclopent-1-enyl-hydroxyphenyl acetic acid (1d): Intermediate (1c) (540 mg, 1.9 mmol) was dissolved in MeOH (927 μL, 22.9 mmol). Water (1.84 mL, 102 mmol) was added, followed by the addition of KOH (1.1 g, 18.8 mmol). The mixture was refluxed at 130° C. for 3 hours, followed by dilution to 250 mL with saturated ammonium chloride, then washed (2×100 mL hexane). The remaining aqueous emulsion was washed (2×250 mL EtOAc). The EtOAc layers were combined, washed with 50 mL saturated aqueous NaCl, dried over Na₂SO₄, filtered and concentrated to yield intermediate (1d) as a brownish-yellow solid (290 mg).

Intermediate (1d) (280 mg, 1.3 mmol) was dissolved in MeOH (2.50 mL, 61.7 mmol) and the reaction flask was flushed with nitrogen before 28 mg of 10% Pd/C was added. The mixture was stirred at room temperature under 1 atm hydrogen and the reaction was monitored by HPLC until the starting material was consumed (˜24 hours). The reaction vessel was flushed with nitrogen, then the mixture was filtered through a pad of Celite® and rinsed with MeOH. The filtrate was concentrated under vacuum to obtain the title compound as a slightly yellow solid (284 mg).

Preparation 2 (R)-2-Cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-phenylethanone

To a stirred solution of (R)-cyclopentylhydroxyphenyl acetic acid (5.00 g, 22.7 mmol) in DCM (200 mL, 3 mol) was added dimethylpiperidin-4-yl amine (2.91 g, 22.7 mmol). DIPEA (11.9 mL, 68.1 mmol) and HOBt (5.21 g, 34 mmol) were added, followed by EDCI (5.22 g, 27.2 mmol). The mixture was stirred for 12 hours, then washed with water (300 mL), a saturated aqueous NaCl solution (300 mL), dried over MgSO₄ and then filtered. The solvent was removed under reduced pressure. The crude material was purified via silica gel chromatography (10% MeOH/DCM w/1% NH₃ (aq)) to afford 4.5 g of the title compound.

Example 1 [1-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin-4-yl]dimethylphenethylammonium

To a stirred solution of (R)-2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-phenylethanone (50 mg, 0.2 mmol) in DMF (1 mL, 10 mmol) was added 1-bromo-2-phenylethane (83 mg, 0.5 mmol). The mixture was heated at 80° C. for 24 hours. The solvent was removed under reduced pressure, and the crude material was purified by preparative HPLC to afford 26.1 mg of the title compound as a TFA salt. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₂, 435.30. found 435.2. ¹H NMR (CD₃OD, 300 MHz) 6 (ppm): 1.04 (1H, m), 1.34 (3H, m), 1.56 (6H, m), 1.89 (1H, m), 2.05 (1H, m), 2.55 (1H, m), 2.83 (2H, m), 3.03 (12H, bm), 3.59 (1H, t), 4.66 (1H, m), 7.19 (1H, d), 7.30 (5H, m) 7.37 (2H, t), 7.41 (2H, d).

Preparation 3 3-(2-Bromoethyl)phenol

A solution of 1-(2-bromoethyl)-3-methoxybenzene (1.00 g, 4.7 mmol) in CHCl₃ (50 mL, 0.6 mol) was cooled to at 0° C. 1.0 M of BBr₃ in DCM (27.9 mL) was cooled to 0° C. and added to the solution. The solution was allowed to warm to 30° C. over 30 minutes, then was poured into a solution of ice and 30% NH₄OH, which was stirred at 0° C. for 30 minutes. The organic layer was taken and concentrated with no reduced pressure.

Example 2 [1-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin-4-yl][2-(3-hydroxyphenyl)ethyl]dimethylammonium

To a stirred solution of (R)-2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-phenylethanone (0.8 g, 2.4 mmol) in DMA (10 mL, 0.1 mol) was added 3-(2-bromoethyl)phenol (1.5 g, 7.3 mmol). The mixture was heated at 80° C. for 24 hours. The solvent was then removed under reduced pressure. The crude material was purified by preparative HPLC to afford 180 mg of the title compound as a TFA salt. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30. found 451.5. ¹H NMR (CD₃OD, 300 MHz) 5 (ppm): 1.17 (1H, m), 1.38 (3H, m), 1.54 (6H, m), 1.89 (1H, m), 2.02 (1H, m), 2.53 (1H, m), 2.79 (2H, m), 2.95 (12H, bm), 3.56 (1H, t), 4.66 (1H, m), 6.70 (3H, m), 7.14 (1H, t) 7.16 (1H, d) 7.29 (2H, t), 7.42 (2H, d).

Example 3

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 3-1 to 3-24, having the following formula, were also prepared:

Ex. R^(Q) Name 3-1 3-fluoro [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(3-fluorophenyl)ethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₈FN₂O₂, 453.29; found 453.4. 3-2 4-fluoro [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(4-fluorophenyl)ethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₈FN₂O₂, 453.29; found 453.4. 3-3 4-hydroxy [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(4-hydroxyphenyl)ethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.4. 3-4 absent [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]dimethylphenethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₂, 435.30; found 435.4. 3-5 2-fluoro [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(2-fluorophenyl)ethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₈FN₂O₂, 453.29; found 453.4. 3-6 2,4- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) dichloro piperidin-4-yl][2-(2,4-dichlorophenyl)ethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₇Cl₂N₂O₂, 503.22; found 503.2. 3-7 2-chloro [2-(2-chlorophenyl)ethyl]-[1-(2-cyclopentyl- 2-hydroxy-2-phenylacetyl)piperidin-4-yl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₈ClN₂O₂, 469.26; found 469.2. 3-8 2-hydroxy- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) ethyl piperidin-4-yl]-{2-[4-(2-hydroxyethyl)phenyl] ethyl}dimethyl-ammonium. MS m/z: [M⁺] calcd for C₃₀H₄₃N₂O₃, 479.33; found 479.4. 3-9 2-chloro-4- [2-(2-chloro-4-fluorophenyl)ethyl][1-(2- fluoro cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin- 4-yl]dimethyl-ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₇ClFN₂O₂, 487.25; found 487.2 3-10 4-methyl [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]dimethyl-(2-p-tolylethyl) ammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₂, 449.32; found 449.4. 3-11 4-bromo [2-(4-bromophenyl)ethyl][1-(2-cyclopentyl- 2-hydroxy-2-phenylacetyl)piperidin-4-yl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₈BrN₂O₂, 513.21; found 513.2. 3-12 4-cyano [2-(4-cyanophenyl)ethyl][1-(2-cyclopentyl- 2-hydroxy-2-phenylacetyl)piperidin-4-yl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₉H₃₈N₃O₂, 460.30; found 460.4. 3-13 4-hydroxy- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) 3-methoxy piperidin-4-yl][2-(4-hydroxy-3-methoxyphenyl) ethyl]dimethyl-ammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₄, 481.31; found 481.4. 3-14 3-methoxy [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(3-methoxyphenyl)ethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₃, 465.31; found 465.4. 3-15 2-bromo [2-(2-bromophenyl)ethyl][1-(2-cyclopentyl- 2-hydroxy-2-phenylacetyl)piperidin-4-yl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₈BrN₂O₂, 513.21; found 513.2. 3-16 4-methoxy [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(4-methoxyphenyl)ethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₃, 465.31; found 465.4. 3-17 absent [(R)-1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) pyrrolidin-3-yl]dimethylphenethylammonium. MS m/z: [M⁺] calcd for C₂₇H₃₇N₂O₂, 421.29; found 421.6. 3-18 4-hydroxy [1-((R)-2-cyclopentyl-2-hydroxy-2- phenylacetyl)piperidin-4-yl]-[2-(4-hydroxyphenyl) ethyl]dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.2. 3-19 4-hydroxy [1-((S)-2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(4-hydroxyphenyl)ethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.2. 3-20 2-fluoro-4- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) methoxy piperidin-4-yl][2-(2-fluoro-4-methoxyphenyl) ethyl]dimethylammonium. MS m/z: [M⁺] calcd for C₂₉H₄₀FN₂O₃, 483.30; found 483.2. 3-21 2-fluoro-4- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) hydroxy piperidin-4-yl][2-(2-fluoro-4-hydroxyphenyl) ethyl]dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₈FN₂O₃, 469.29; found 469.2. 3-22 3-hydroxy [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(3-hydroxyphenyl)ethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.2. 3-23 3-fluoro [1-((R)-2-cyclopentyl-2-hydroxy-2- phenylacetyl)piperidin-4-yl][2-(3-fluorophenyl) ethyl]dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₈FN₂O₂, 453.29; found 453.2. 3-24 2-hydroxy [1-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(2-hydroxyphenyl)ethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.2.

Example 4

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 4-1 to 4-8, having the following formula, were also prepared:

Ex. Q Name 4-1 1H-indol-3-yl [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(1H-indol-3-yl)ethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₃₀H₄₀N₃O₂, 474.31; found 474.4. 4-2 thiophen-2-yl [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]dimethyl(2-thiophen-2-ylethyl) ammonium. MS m/z: [M⁺] calcd for C₂₆H₃₇N₂O₂S, 441.26; found 441.2. 4-3 benzo[1,3] (2-benzo[1,3]dioxol-5-ylethyl)[1-(2-cyclopentyl- dioxol-5-yl 2-hydroxy-2-phenylacetyl)piperidin-4-yl]dimethyl- ammonium. MS m/z: [M⁺] calcd for C₂₉H₃₉N₂O₄, 479.29; found 479.4. 4-4 thiophen-3-yl [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]dimethyl(2-thiophen-3-ylethyl) ammonium. MS m/z: [M⁺] calcd for C₂₆H₃₇N₂O₂S, 441.26; found 441.2. 4-5 pyrrol-1-yl [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]dimethyl(2-pyrrol-1-ylethyl) ammonium. MS m/z: [M⁺] calcd for C₂₆H₃₈N₃O₂, 424.30; found 424.4. 4-6 1H-tetrazol- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) 5-yl piperidin-4-yl]dimethyl[2-(1H-tetrazol-5-yl)ethyl] ammonium. MS m/z: [M⁺] calcd for C₂₃H₃₅N₆O₂, 427.28; found 427.2. 4-7 thiophen-3-yl [1-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]dimethyl-(2-thiophen-3-ylethyl) ammonium. MS m/z: [M⁺] calcd for C₂₆H₃₇N₂O₂S, 441.26; found 441.2. 4-8 thiophen-2-yl [1-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]dimethyl(2-thiophen-2-ylethyl) ammonium. MS m/z: [M⁺] calcd for C₂₆H₃₇N₂O₂S, 441.26; found 441.2.

Example 5

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 5-1 to 5-3, having the following formula, were also prepared:

Ex. R Name 5-1 phenyl (2-cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin- 4-yl]-(3,3-diphenylpropyl)dimethylammonium. MS m/z: [M⁺] calcd for C₃₅H₄₅N₂O₂, 525.35; found 525.4. 5-2 —OH [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin- 4-yl]-((R)-2-hydroxy-2-phenylethyl)dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.2. 5-3 —OH [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin- 4-yl]-((S)-2-hydroxy-2-phenylethyl)dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.2.

Example 6

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 6-1 to 6-14, having the following formula, were also prepared:

Ex. R^(Q) Name 6-1 2- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piper- methoxy- idin-4-yl](2-methoxy-4-methoxy-carbonylbenzyl) 4- dimethylammonium. MS m/z: [M⁺] calcd for methoxy- C₃₀H₄₁N₂O₅ 509.30; found 509.4. carbonyl 6-2 4- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piper- trifluoro- idin-4-yl]dimethyl-(4-trifluoromethoxybenzyl) methoxy ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₆F₃N₂O₃, 505.27; found 505.4. 6-3 4-chloro (4-chlorobenzyl)-[1-(2-cyclopentyl-2-hydroxy-2- phenylacetyl)piperidin-4-yl]dimethylammonium. MS m/z: [M⁺] calcd for C₂₇H₃₆ClN₂O₂, 455.25; found 455.2. 6-4 3-fluoro [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piper- idin-4-yl](3-fluorobenzyl)dimethylammonium. MS m/z: [M⁺] calcd for C₂₇H₃₆FN₂O₂, 439.28; found 439.4. 6-5 3-nitro [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piper- idin-4-yl]dimethyl(3-nitrobenzyl)ammonium. MS m/z: [M⁺] calcd for C₂₇H₃₆N₃O₄, 466.27; found 466.4. 6-6 4-t-butyl (4-t-butylbenzyl)[1-(2-cyclopentyl-2-hydroxy-2- phenylacetyl)piperidin-4-yl]-dimethylammonium. MS m/z: [M⁺] calcd for C₃₁H₄₅N₂O₂, 477.35; found 477.4. 6-7 4- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piper- trifluoro- idin-4-yl]dimethyl(4-trifluoromethylbenzyl) methyl ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₆F₃N₂O₂, 489.27; found 489.4. 6-8 4-bromo (4-bromobenzyl)[1-(2-cyclopentyl-2-hydroxy-2- phenylacetyl)piperidin-4-yl]dimethylammonium. MS m/z: [M⁺] calcd for C₂₇H₃₆BrN₂O₂, 499.20; found 499.2. 6-9 4-cyano (4-cyanobenzyl)-[1-(2-cyclopentyl-2-hydroxy-2- phenylacetyl)piperidin-4-yl]dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₆N₃O₂, 446.28; found 446.4. 6-10 4-fluoro [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)-piper- idin-4-yl] (4-fluorobenzyl)dimethylammonium. MS m/z: [M⁺] calcd for C₂₇H₃₆FN₂O₂, 439.28; found 439.4. 6-11 4-methyl [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piper- idin-4-yl]dimethyl(4-methylbenzyl)ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₂, 435.30; found 435.4. 6-12 3-methyl [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piper- idin-4-yl]dimethyl(3-methylbenzyl) ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₂, 435.30; found 435.4. 6-13 4-nitro [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piper- idin-4-yl]dimethyl(4-nitrobenzyl)ammonium. MS m/z: [M⁺] calcd for C₂₇H₃₆N₃O₄, 466.27; found 466.4. 6-14 4- (4-carboxymethylbenzyl)[1-(2-cyclopentyl- carboxy- 2-hydroxy-2-phenylacetyl)piperidin-4-yl] methyl dimethylammonium. MS m/z: [M⁺] calcd for C₂₉H₃₉N₂O₄, 479.29; found 479.4.

Example 7

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 7-1 to 7-11, having the following formula, were also prepared:

Ex. R^(Q) Name 7-1 absent [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin- 4-yl]dimethyl(2-oxo-2-phenylethyl)ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₇N₂O₃, 449.28; found 449.3. 7-2 4-bromo [2-(4-bromophenyl)-2-oxoethyl]-[1-(2-cyclopentyl-2- hydroxy-2-phenylacetyl)piperidin-4-yl]dimethyl- ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₆BrN₂O₃, 528.19; found 529.2. 7-3 4- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin- methoxy 4-yl]-[2-(4-methoxyphenyl)-2-oxoethyl]dimethyl- ammonium. MS m/z: [M⁺] calcd for C₂₉H₃₉N₂O₄, 479.29; found 479.2. 7-4 3-cyano [2-(3-cyanophenyl)-2-oxoethyl][1-(2-cyclopentyl- 2-hydroxy-2-phenylacetyl)piperidin-4-yl]dimethyl- ammonium. MS m/z: [M⁺] calcd for C₂₉H₃₆N₃O₃, 474.28; found 474.2. 7-5 4-cyano [2-(4-cyanophenyl)-2-oxoethyl][1-(2-cyclopentyl- 2-hydroxy-2-phenylacetyl)piperidin-4-yl]dimethyl- ammonium. MS m/z: [M⁺] calcd for C₂₉H₃₆N₃O₃, 474.28; found 474.2. 7-6 4-chloro [2-(4-chlorophenyl)-2-oxoethyl][1-(2-cyclopentyl- 2-hydroxy-2-phenylacetyl)piperidin-4-yl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₆ClN₂O₃, 483.24; found 483.2. 7-7 3-fluoro [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(3-fluorophenyl)-2-oxoethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₆FN₂O₃, 467.27; found 467.2. 7-8 2- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) methoxy piperidin-4-yl][2-(2-methoxyphenyl)-2-oxoethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₉H₃₉N₂O₄, 479.29; found 479.2. 7-9 4- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin- difluoro- 4-yl][2-(4-difluoromethoxyphenyl)-2-oxoethyl] methoxy dimethyl-ammonium. MS m/z: [M⁺] calcd for C₂₉H₃₇F₂N₂O₄, 515.27; found 515.2. 7-10 3- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin- methoxy 4-yl][2-(3-methoxyphenyl)-2-oxoethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₉H₃₉N₂O₄, 479.29; found 479.2. 7-11 2-chloro [2-(2-chlorophenyl)-2-oxoethyl][1-(2-cyclopentyl- 2-hydroxy-2-phenylacetyl)piperidin-4-yl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₆ClN₂O₃, 483.24; found 483.2.

Example 8

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 8-1 to 8-4, having the following formula, were also prepared:

Ex. a R^(Q) Name 8-1 2 absent [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]dimethyl-(2-phenoxyethyl) ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.4. 8-2 4 absent [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]dimethyl-(4-phenoxybutyl) ammonium. MS m/z: [M⁺] calcd for C₃₀H₄₃N₂O₃, 479.33; found 479.4. 8-3 3 absent [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]dimethyl-(3-phenoxypropyl) ammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₃, 465.31; found 465.4. 8-4 2 4-fluoro [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(4-fluorophenoxy)ethyl]dimethyl ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₈FN₂O₃, 469.29; found 469.4.

Example 9

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 9-1 to 9-10, having the following formula, were also prepared:

Ex. a b R^(Q) Name 9-1 1 1 absent benzyl-[1-(2-cyclopentyl-2-hydroxy-2- phenylacetyl)-piperidin-4-ylmethyl] dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₂, 435.30; found 435.2. 9-2 1 2 absent [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-ylmethyl]dimethylphenethyl- ammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₂, 449.32; found 449.2. 9-3 1 3 absent [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-ylmethyl]dimethyl(3-phenylpropyl) ammonium. MS m/z: [M⁺] calcd for C₃₀H₄₃N₂O₂, 463.33; found 463.2. 9-4 1 1 3-methyl [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-ylmethyl]dimethyl(3-methylbenzyl) ammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₂, 449.32; found 449.2. 9-5 1 1 2- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) hydroxy piperidin-4-ylmethyl](2-hydroxybenzyl) dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.2. 9-6 1 1 3- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) hydroxy piperidin-4-ylmethyl](3-hydroxybenzyl) dimethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.0. 9-7 1 1 4- [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) hydroxy piperidin-4-ylmethyl]-4-hydroxybenzyl)dimethyl- ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.0. 9-8 0 3 absent [(R)-1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)- pyrrolidin-3-yl]dimethyl(3-phenylpropyl) ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₂, 435.30; found 435.2. 9-9 0 2 4-carboxy [2-(4-carboxyphenyl)ethyl][1-((R)-2-cyclopentyl- 2-hydroxy-2-phenylacetyl)piperidin-4-yl] dimethyl-ammonium. MS m/z: [M⁺] calcd for C₂₉H₃₉N₂O₄, 479.29. 9-10 0 2 4- [1-((R)-2-cyclopentyl-2-hydroxy-2-phenylacetyl) methoxy- piperidin-4-yl]-[2-(4-methoxycarbonylphenyl) carbonyl ethyl]dimethyl-ammonium. MS m/z: [M⁺] calcd for C₃₀H₄₁N₂O₄, 493.31.

Example 10

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 10-1 to 10-6, having the following formula, were also prepared:

Ex. R⁶ Name 10-1 —CH₂CH₃ [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]ethyl-[2-(4-hydroxyphenyl) ethyl]methylammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₃, 465.31; found 465.2. 10-2 —(CH₂)₂CH₃ [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(4-hydroxyphenyl)ethyl] methylpropylammonium. MS m/z: [M⁺] calcd for C₃₀H₄₃N₂O₃, 479.33; found 479.4. 10-3 —CH₂-cyclopropyl [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl]cyclopropylmethyl[2-(4- hydroxyphenyl)ethyl]methylammonium. MS m/z: [M⁺] calcd for C₃₁H₄₃N₂O₃, 491.33; found 481.4. 10-4 —(CH₂)₂OH [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl](2-hydroxyethyl)[2-(4- hydroxy-phenyl)ethyl]methylammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₄, 481.31; found 491.4. 10-5 —CH₂—C(O)OCH₃ [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl) piperidin-4-yl][2-(4-hydroxyphenyl)ethyl] methoxycarbonylmethylmethylammonium. MS m/z: [M⁺] calcd for C₃₀H₄₁N₂O₅, 509.30; found 509.2. 10-6 —CH₂—C(O)NH₂ carbamoylmethyl[1-(2-cyclopentyl-2- hydroxy-2-phenylacetyl)piperidin-4-yl][2- (4-hydroxy-phenyl)ethyl]methylammonium. MS m/z:[M⁺] calcd for C₂₉H₄₀N₃O₄, 494.30; found 494.2.

Example 11

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 11-1 to 11-3, having the following formula, were also prepared:

Ex. b Name 11-1 2 [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)azetidin-3-yl] dimethylphenethyl ammonium. MS m/z: [M⁺] calcd for C₂₆H₃₅N₂O₂, 407.27; found 407.2. 11-2 3 [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)azetidin-3-yl] dimethyl(3-phenylpropyl)ammonium. MS m/z: [M⁺] calcd for C₂₇H₃₇N₂O₂, 421.29; found 421.2. 11-3 4 [1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)azetidin-3-yl] dimethyl(4-phenylbutyl)ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₂, 435.30; found 435.4.

Example 12

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, the following compound was also prepared:

[1-(2-cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin-4-yl]dimethyl(2-pyrazol-1-ylethyl)ammonium. MS m/z: [M⁺] calcd for C₂₅H₃₇N₄O₂, 425.29. found 425.6.

Example 13 [1-((R)-2-Cyclopentyl-2-hydroxy-2-phenylacetyl)piperidin-4-yl][2-(2-fluorophenyl)ethyl]dimethylammonium (13-1) and [1-(2-Cyclopentylidene-2-phenylacetyl)piperidin-4-yl]-[2-(2-fluorophenyl)ethyl]dimethylammonium (13-2)

To a stirred solution of (R)-2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-phenylethanone (50 mg, 0.2 mmol) in DMF (1 mL, 10 mmol), was added 1-(2-bromoethyl)-2-fluorobenzene (91 mg, 0.5 mmol). The mixture was heated at 80° C. for 24 hours. The solvent was removed under reduced pressure, and the crude material was purified by preparative HPLC to afford 12.2 mg of compound (13-1) as a TFA salt. Additionally the eliminated compound was obtained during the preparative HPLC to afford 18.6 mg of compound (13-2).

(13-1) MS m/z: [M⁺] calcd for C₂₈H₃₈FN₂O₂, 453.29. found 453.2.

(13-2) MS m/z: [M⁺] calcd for C₂₈H₃₆FN₂O, 435.28. found 435.4.

Preparation 4 2-Cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-thiophen-2-ylethanone

1-(4-Dimethylaminopiperidin-1-yl)-2-thiophen-2-yl-ethane-1,2-dione (4a): 2-Thiopheneglyoxylic acid (300 mg, 1.9 mmol) was dissolved in 10 mL of methylene chloride. A 2.0 M solution of oxalyl chloride in methylene chloride (1.1 mL, 2.1 mmol) was then added, followed by 10 μL of DMF. The resulting solution was stirred at room temperature for 1 hour, then a solution of dimethylpiperidin-4-ylamine (271 mg, 2.1 mmol) and DIPEA (1.0 mL, 5.8 mmol) in 2 mL of methylene chloride was added. 4-Dimethylaminopyridine (12 mg, 96 μmol) was then added and the resulting mixture was stirred at room temperature for 2 hours. The mixture was then extracted with a saturated sodium bicarbonate solution, and the organic layer was dried over Na₂SO₄ and concentrated to yield the crude intermediate (4a) (498 mg), which was used in the next step without further purification.

Intermediate (4a) (498 mg, 1.87 mmol) was dissolved in 10 mL of THF, and the solution was cooled to 0° C. A 2.0 M solution of cyclopentyl magnesium bromide in ether (1.12 mL, 2.24 mmol) was added slowly and the mixture was stirred at 0° C. for 4 hours. The mixture was then quenched by the addition saturated ammonium chloride solution. The resulting mixture was extracted with EtOAc, then the organic layer was dried over Na₂SO₄ and concentrated to yield the crude title compound (406 mg), which was used in the next step without further purification.

Example 14 [1-(2-Cyclopentyl-2-hydroxy-2-thiophen-2-yl-acetyl)piperidin-4-yl]-[2-(4-hydroxy-phenyl)ethyl]dimethylammonium

(2-Cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-thiophen-2-ylethanone (75 mg, 220 μmol) was dissolved in 1 mL of DMF. DIPEA (104 μL, 594 μmol) and 4-(2-bromoethyl)phenol (89.6 mg, 446 μmol) were then added and the mixture was stirred at 60° C. for 8 hours. The mixture was then concentrated, after which the residue was dissolved in a 1:1 mixture of water and acetonitrile and purified by liquid chromatography. 1.6 mg of the trifluoroacetate salt of the title compound was isolated as a white powder. MS m/z: [M⁺] calcd for C₂₆H₃₇N₂O₃S; 457.25 found 457.2.

Example 15

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 15-1 to 15-3, having the following formula, were also prepared:

Ex. R^(Q) Name 15-1 absent [1-(2-cyclopentyl-2-hydroxy-2-thiophen-2-ylacetyl)piperidin- 4-yl]dimethylphenethylammonium. MS m/z: [M⁺] calcd for C₂₆H₃₇N₂O₂S, 441.26; found 441.5. 15-2 3- [1-(2-cyclopentyl-2-hydroxy-2-thiophen-2-ylacetyl)piperidin- fluoro 4-yl]-[2-(3-fluorophenyl)ethyl]dimethylammonium. MS m/z: [M⁺] calcd for C₂₆H₃₆FN₂O₂S, 459.25; found 459.2. 15-3 4- [1-(2-cyclopentyl-2-hydroxy-2-thiophen-2-ylacetyl)piperidin- fluoro 4-yl]-[2-(4-fluorophenyl)ethyl]dimethylammonium. MS m/z: [M⁺] calcd for C₂₆H₃₆FN₂O₂S, 459.25; found 459.2.

Preparation 5 1-(4-Dimethylamino-piperidin-1-yl)-2-hydroxy-4-methyl-2-phenylpentan-1-one

1-(4-Dimethylamino-piperidin-1-yl)-2-phenylethane-1,2-dione (5a): Benzoylformic acid (1.0 g, 6.7 mmol), dimethylpiperidin-4-ylamine (854 mg, 6.7 mmol), DIPEA (3.5 mL, 20.0 mmol), and 1-hydroxybenzotriazole (1.4 g, 10 mmol) were dissolved in 20 mL of methylene chloride, then N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (1.53 g, 7.99 mmol) was added and the mixture was stirred at room temperature for 16 hours. The mixture was extracted with a 1.0 N NaOH solution, then the organic layer was dried over Na₂SO₄ and concentrated. The crude product was purified by column chromatography (10-30% MeOH in methylene chloride gradient) to give intermediate (5a) (501 mg).

Intermediate (5a) (75.0 mg, 288 μmol) was dissolved in 2 mL of THF, and the solution was cooled to 0° C. A 2.0 M solution of isobutyl magnesium bromide in ether (158 μL, 317 μmol) was added slowly and the mixture was stirred at 0° C. for 4 hours. The mixture was then quenched by the addition of a saturated sodium bicarbonate solution. The resulting mixture was extracted with EtOAc, then the organic layer was dried over Na₂SO₄ and concentrated to give the crude title compound, which was used in the next step without further purification.

Example 16 [1-(2-Hydroxy-4-methyl-2-phenylpentanoyl)piperidin-4-yl]dimethylphenethylammonium

1-(4-dimethylamino-piperidin-1-yl)-2-hydroxy-4-methyl-2-phenylpentan-1-one was dissolved in 1 mL of DMF and 1-bromo-2-phenylethane (43.3 μL, 317 μmol) was added. The mixture was then microwaved (140° C., 300 watts, 7 minutes), after which the mixture was concentrated. The residue was then dissolved in a 1:1 mixture of water and acetonitrile and purified by liquid chromatography. 4.7 mg of the trifluoroacetate salt of the title compound was isolated as a white powder. MS m/z: [M⁺] calcd for C₂₇H₃₉N₂O₂, 423.30. found 423.2.

Example 17

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 17-1 and 17-2, having the following formula, were also prepared:

Ex. R¹ R³ Name 17-1 cyclopropyl —OH [1-(2-cyclopropyl-2-hydroxy-2- phenylacetyl)-piperidin-4-yl] dimethylphenethylammonium. MS m/z: [M⁺] calcd for C₂₆H₃₅N₂O₂, 407.27; found 407.2. 17-2 —CH₂—CH═CH₂ —OH [1-(2-hydroxy-2-phenyl-pent-4- enoyl)piperidin-4-yl] dimethylphenethylammonium. MS m/z: [M⁺] calcd for C₂₆H₃₅N₂O₂, 407.27; found 407.2. 17-3 cyclopropyl —CH₂—OH [1-(2-cyclopentyl-3-hydroxy-2- phenylpropionyl)-piperidin-4-yl] dimethylphenethylammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₂, 450.32; found 449.2. 17-4 —(CH₂)₂—SCH₃ H dimethyl-[1-(4-methylsulfanyl-2- phenylbutyryl)-piperidin-4-yl] phenethylammonium. MS m/z: [M⁺] calcd for C₂₆H₃₇N₂OS, 426.26; found 426.5. 17-5 —(CH₂)₂—SCH₃ —CH₂—OH [1-(2-hydroxymethyl-4-methyl- sulfanyl-2-phenylbutyryl) piperidin-4-yl]dimethyl phenethyl-ammonium. MS m/z: [M⁺] calcd for C₂₇H₃₉N₂O₂S, 456.27; found 456.2. 17-6 —C≡CH —OH [1-(2-hydroxy-2-phenylbut-3- ynoyl)piperidin-4-yl] dimethylphenethylammonium. MS m/z: [M⁺] calcd for C₂₅H₃₁N₂O₂, 392.24; found 391.5.

Preparation 6 1-(4-Dimethylamino-piperidin-1-yl)-2-hydroxy-2,2-di-thiophen-2-ylethanone

To a stirred solution of 2-thiopheneglyoxylic acid (1.0 g, 6.4 mmol) in DCM (100 mL, 2 mol), was added oxalyl chloride (596 μL, 7 mmol) and a catalytic amount of DMF. The mixture was stirred for 2 hours and then was cooled at 0° C. in an ice bath. Dimethyl-piperidin-4-ylamine (821 mg, 6.4 mmol), DIPEA (1.7 mL, 9.6 mmol) and DMAP (20 mg, 0.1 mmol) were added, and the mixture was stirred for 2 hours. The solvent was removed under reduced pressure and the crude mixture was then dissolved in DCM (60 mL), washed with a saturated bicarbonate solution (50 mL), and dried over MgSO₄. The solvent was removed under reduced pressure and the crude material was then dissolved in THF (50 mL, 0.6 mol) and cooled to 0° C. in an ice bath. To the stirred solution was added 1.0 M thiophen-2-yl magnesium bromide in THF (7.7 mL, 7.7 mmol) was added. The mixture was stirred for 30 minutes, then quenched with a saturated bicarbonate solution (50 mL) and DCM (50 mL). The organic was taken and dried over MgSO₄, and the solvent was removed under reduced pressure, to afford the title compound (1.5 g).

MS m/z: [M⁴] calcd for C₁₇H₂₂N₂O₂S₂, 350.50. found 351.4.

Example 18 [2-(2-Fluorophenyl)ethyl]-[1-(2-hydroxy-2,2-di-thiophen-2-ylacetyl) piperidin-4-yl]dimethylammonium

The title compound was prepared using the procedure described in Example 13, and replacing (R)-2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-phenylethanone with 1-(4-dimethylamino-piperidin-1-yl)-2-hydroxy-2,2-di-thiophen-2-ylethanone. MS m/z: [M⁺] calcd for C₂₅H₃₀FN₂O₂S₂, 473.17. found 473.2.

Example 19

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 19-1 to 19-4, having the following formula, were also prepared:

Ex. Q Name 19-1

[1-(2-hydroxy-2,2-dithiophen-2-yl-acetyl)piperidin-4-yl] dimethylphenethylammonium. MS m/z: [M⁺] calcd for C₂₅H₃₁N₂O₂S₂, 455.18; found 455.2. 19-2

(2-benzo[1,3]dioxol-5-yl-ethyl)-[1-(2-hydroxy-2,2- dithiophen-2-ylacetyl)piperidin-4-yl]dimethyl-ammonium. MS m/z: [M⁺] calcd for C₂₆H₃₁N₂O₄S₂, 499.17; found 499.2. 19-3

[1-(2-hydroxy-2,2-dithiophen-2-yl-acetyl)piperidin-4-yl] dimethyl(2-m-tolylethyl)ammonium. MS m/z: [M⁺] calcd for C₂₆H₃₃N₂O₂S₂, 469.20; found 469.2. 19-4

[1-(2-hydroxy-2,2-dithiophen-2-yl-acetyl)piperidin-4-yl] dimethyl(2-p-tolylethyl)ammonium. MS m/z: [M⁺] calcd for C₂₆H₃₃N₂O₂S₂, 469.20; found 469.2.

Example 20 [1-(2-Cyclopentyl-2-phenylacetyl)piperidin-4-yl]dimethylphenethylammonium

The title compound was synthesized using the procedure described in Example 1 and using 2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-phenylethanone instead of (R)-2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-phenylethanone. 2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-phenylethanone was prepared as described in Preparation 2, using α-cyclopentylphenyl acetic acid instead of (R)-cyclopentylhydroxyphenyl acetic acid as the starting material. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O, 419.31. found 419.2.

Preparation 7 2-Cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-p-tolylethanone

The title compound was synthesized using the procedure described in Preparation 6, and replacing 2-thiopheneglyoxylic acid with (4-methylphenyl)(oxo)acetic acid, and replacing 1.0 M thiophen-2-yl magnesium bromide in THF with 2.0 M cyclopentyl magnesium bromide in ether.

Example 21 [1-(2-Cyclopentyl-2-hydroxy-2-p-tolylacetyl)piperidin-4-yl]dimethylphenethylammonium

The title compound was synthesized using the procedure described in Example 13, and replacing (R)-2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-phenylethanone with 2-cyclopentyl-1-(4-dimethylaminopiperidin-1-yl)-2-hydroxy-2-p-tolylethanone. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₂, 449.32. found 449.2

Example 22

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 22-1 to 22-5, having the following formula, were also prepared:

Ex. R² Name 22-1

{1-[2-cyclopentyl-2-hydroxy-2-(3-hydroxyphenyl)-acetyl] piperidin-4-yl}dimethylphenethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₉N₂O₃, 451.30; found 451.2. 22-2

{1-[2-cyclopentyl-2-(3-fluoro-4-methoxyphenyl)-2-hydroxy- acetyl]-piperidin-4-yl}dimethylphenethyl-ammonium. MS m/z: [M⁺] calcd for C₂₉H₄₀FN₂O₃, 483.30; found 483.2. 22-3

{1-[2-cyclopentyl-2-(4-fluorophenyl)-2-hydroxy-acetyl] piperidin-4-yl}dimethyl-phenethylammonium. MS m/z: [M⁺] calcd for C₂₈H₃₈FN₂O₂, 453.29; found 453.2. 22-4

[1-(2-cyclopentyl-2-hydroxy-2-m-tolylacetyl)-piperidin-4-yl] dimethylphenethylammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₂, 449.32; found 449.2. 22-5

[1-(2-cyclopentyl-2-hydroxy-2-o-tolylacetyl)-piperidin-4-yl] dimethylphenethylammonium. MS m/z: [M⁺] calcd for C₂₉H₄₁N₂O₂, 449.32; found 449.2.

Preparation 8 (4-Dimethylaminopiperidin-1-yl)(9H-xanthen-9-yl)methanone

To a stirred solution of 9H-xanthene-9-carboxylic acid (4.4 g, 19.4 mmol) in DCM (200 mL, 3 mol) was added dimethylpiperidin-4-yl-amine (2.5 g, 19.4 mmol). DIPEA (6.8 mL, 38.9 mmol) and HOBt (4.6 g, 34 mmol) were added to the mixture, followed by EDCI (4.5 g, 23.3 mmol). The mixture was stirred for 12 hours, then washed with water (300 mL), NaCl (sat.) (300 mL), dried over MgSO₄ and then filtered. The solvent was removed under reduced pressure, and the crude material was purified via silica gel chromatography (10% MeOH/DCM w/1% NH₃ (aq)) to yield the title compound (5.9 g).

Example 23 [2-(2-Fluorophenyl)ethyl]dimethyl-[1-(9H-xanthene-9-carbonyl)piperidin-4-yl]ammonium

To a stirred solution of (4-dimethylaminopiperidin-1-yl)(9H-xanthen-9-yl)methanone (50 mg; 0.2 mmol) in DMF (1 mL, 10 mmol) was added 1-(2-bromoethyl)-2-fluorobenzene (30 mg, 0.2 mmol). The mixture was heated at 80° C. for 24 hours. The solvent was removed under reduced pressure, and the crude material was purified by preparative HPLC to yield the title compound as a TFA salt (36.7 mg). MS m/z: [M⁺] calcd for C₂₉H₃₂FN₂O₂, 460.24. found 459.2.

Example 24

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 24-1 to 24-4, having the following formula, were also prepared:

Ex. b Z Q Name 24-1 2 bond

[2-(4-hydroxyphenyl)ethyl]dimethyl-[1-(9H- xanthene-9-carbonyl)piperidin-4- yl]ammonium. MS m/z: [M⁺] calcd for C₂₉H₃₃N₂O₃, 458.25; found 457.2. 24-2 2 bond

dimethyl-(2-thiophen-3-ylethyl)-1[1-(9H- xanthene-9-carbonyl)piperidin-4- yl]ammonium. MS m/z: [M⁺] calcd for C₂₇H₃₁N₂O₂S, 448.21; found 447.2. 24-3 1 —C(O)—

dimethyl-(2-oxo-2-phenylethyl)-[1-(9H- xanthene-9-carbonyl)piperidin-4- yl]ammonium. MS m/z: [M⁺] calcd for C₂₉H₃₁N₂O₃, 456.23; found 455.2. 24-4 2 bond

dimethylphenethyl-[1-(9H-xanthene-9- carbonyl)piperidin-4-yl]ammonium. MS m/z: [M⁺] calcd for C₂₉H₃₃N₂O₂, 442.25; found 441.2.

Example 25

Following the procedures described in the examples above, and substituting the appropriate starting materials and reagents, compounds 25-1 to 25-3, having the following formula, were also prepared:

Ex. b Name 24-1 2 dimethylphenethyl-[1-(9H-xanthene-9-carbonyl) azetidin-3-yl]ammonium. MS m/z: [M⁺] calcd for C₂₇H₂₉N₂O₂, 414.22; found 413.2. 24-2 3 dimethyl-(3-phenylpropyl)-[1-(9H-xanthene-9- carbonyl)azetidin-3-yl]ammonium. MS m/z: [M⁺] calcd for C₂₈H₃₁N₂O₂, 428.24; found 427.2. 24-3 4 dimethyl-(4-phenylbutyl)-[1-(9H-xanthene-9- carbonyl)azetidin-3-yl]ammonium. MS m/z: [M⁺] calcd for C₂₉H₃₃N₂O₂, 442.25; found 441.2.

Assay 1 Radioligand Binding Assay Membrane Preparation from Cells Expressing hM₁, hM₂, hM₃ and hM₄ Muscarinic Receptor Subtypes

Chinese hamster ovary (CHO) cell lines stably expressing cloned human hM₁, hM₂, hM₃ and hM₄ muscarinic receptor subtypes, respectively, were grown to near confluency in medium consisting of HAM's F-12 supplemented with 10% fetal bovine serum and 250 μg/mL Geneticin. The cells were grown in a 5% CO₂, 37° C. incubator and lifted with 2 mM EDTA in dPBS. Cells were collected by 5 minute centrifugation at 650×g, and cell pellets were either stored frozen at −80° C. or membranes were prepared immediately. For membrane preparation, cell pellets were resuspended in lysis buffer and homogenized with a Polytron PT-2100 tissue disrupter (Kinematica AG; 20 seconds×2 bursts). Crude membranes were centrifuged at 40,000×g for 15 minutes at 4° C. The membrane pellet was then resuspended with resuspension buffer and homogenized again with the Polytron tissue disrupter. The protein concentration of the membrane suspension was determined by the method described in Lowry, O. et al., Journal of Biochemistry 193:265 (1951). All membranes were stored frozen in aliquots at −80° C. or used immediately. Aliquots of prepared hM₅ receptor membranes were purchased directly from Perkin Elmer and stored at −80° C. until use.

Radioligand Binding Assay on Muscarinic Receptor Subtypes hM₁, hM₂, hM₃, hM₄ and hM₅

Radioligand binding assays were performed in 96-well microtiter plates in a total assay volume of 1000 μL. CHO cell membranes stably expressing either the hM₁, hM₂, hM₃, hM₄ or hM₅ muscarinic subtype were diluted in assay buffer to the following specific target protein concentrations (μg/well): 10 μg for hM₁, 10-15 μg for hM₂, 10-20 μg for hM₃, 10-20 μg for hM₄, and 10-12 μg for hM₅. The membranes were briefly homogenized using a Polytron tissue disruptor (10 seconds) prior to assay plate addition. Saturation binding studies for determining K_(D) values of the radioligand were performed using L-[N-methyl-³H]scopolamine methyl chloride ([³H]-NMS) (TRK666, 84.0 Ci/mmol, Amersham Pharmacia Biotech, Buckinghamshire, England) at concentrations ranging from 0.001 nM to 20 nM. Displacement assays for determination of K_(i) values of test compounds were performed with [³H]-NMS at 1 nM and eleven different test compound concentrations. The test compounds were initially dissolved to a concentration of 40 μM in dilution buffer and then serially diluted 5× with dilution buffer to final concentrations ranging from 400 fM to 4 μM. The addition order and volumes to the assay plates were as follows: 825 pt assay buffer with 0.1% BSA, 25 μL radioligand, 100 μL diluted test compound, and 50 μL membranes. Assay plates were incubated for 6 hours at 37° C. Binding reactions were terminated by rapid filtration over GF/B glass fiber filter plates (Perkin Elmer Inc., Wellesley, Mass.) pre-treated in 0.3% polyethyleneimine. Filter plates were rinsed three times with wash buffer (10 mM HEPES) to remove unbound radioactivity. Plates were then air dried, and 50 μL Microscint-20 liquid scintillation fluid (PerkinElmer Inc., Wellesley, Mass.) was added to each well. The plates were then counted in a PerkinElmer Topcount liquid scintillation counter (PerkinElmer Inc., Wellesley, Mass.). Binding data were analyzed by nonlinear regression analysis with the GraphPad Prism Software package (GraphPad Software, Inc., San Diego, Calif.) using the one-site competition model. K_(i) values for test compounds were calculated from observed IC₅₀ values and the K_(D) value of the radioligand using the Cheng-Prusoff equation (Cheng Y; Prusoff W. H. Biochemical Pharmacology 22(23):3099-108 (1973)). K_(i) values were converted to pK_(i) values to determine the geometric mean and 95% confidence intervals. These summary statistics were then converted back to K_(i) values for data reporting.

In this assay, a lower K_(i) value indicates that the test compound has a higher binding affinity for the receptor tested. Exemplary compounds of the invention that were tested in this assay, were found to have a K_(i) value of less than about 100 nM for the M₃ muscarinic receptor subtype in this assay. More typically, these compounds were found to have K_(i) values of less than about 50 nM, with some compounds having K_(i) values of less than about 10 nM or less than about 1.0 nM. For example, the compounds of Example 1 and Example 2 exhibited a K_(i) value of less than about 1.0 nM for the M₃ muscarinic receptor subtype in this assay.

Assay 2 Muscarinic Receptor Functional Potency Assays Blockade of Agonist-Mediated Inhibition of cAMP Accumulation

In this assay, the functional potency of a test compound is determined by measuring the ability of the test compound to block oxotremorine-inhibition of forskolin-mediated cAMP accumulation in CHO-K1 cells expressing the hM₂ receptor.

cAMP assays are performed in a radioimmunoassay format using the Flashplate Adenylyl Cyclase Activation Assay System with ¹²⁵I-cAMP (NEN SMP004B, PerkinElmer Life Sciences Inc., Boston, Mass.), according to the manufacturer's instructions.

Cells are rinsed once with dPBS and lifted with Trypsin-EDTA solution (0.05% trypsin/0.53 mM EDTA) as described in Assay 1. The detached cells are washed twice by centrifugation at 650×g for five minutes in 50 mLs dPBS. The cell pellet is then re-suspended in 10 mL dPBS, and the cells are counted with a Coulter Z1 Dual Particle Counter (Beckman Coulter, Fullerton, Calif.). The cells are centrifuged again at 650×g for five minutes and re-suspended in stimulation buffer to an assay concentration of 1.6×10⁶-2.8×10⁶ cells/mL.

The test compound is initially dissolved to a concentration of 400 μM in dilution buffer (dPBS supplemented with 1 mg/mL BSA (0.1%)), and then serially diluted with dilution buffer to final molar concentrations ranging from 100 μM to 0.1 nM. Oxotremorine is diluted in a similar manner.

To measure oxotremorine inhibition of adenylyl cyclase (AC) activity, 25 μL forskolin (25 μM final concentration diluted in dPBS), 25 μL diluted oxotremorine, and 50 μL cells are added to agonist assay wells. To measure the ability of a test compound to block oxotremorine-inhibited AC activity, 25 μL forskolin and oxotremorine (25 μM and 5 μM final concentrations, respectively, diluted in dPBS) 25 μL diluted test compound, and 50 μL cells are added to remaining assay wells.

Reactions are incubated for 10 minutes at 37° C. and stopped by addition of 100 μL ice-cold detection buffer. Plates are sealed, incubated overnight at room temperature and counted the next morning on a PerkinElmer TopCount liquid scintillation counter (PerkinElmer Inc., Wellesley, Mass.). The amount of cAMP produced (pmol/well) is calculated based on the counts observed for the samples and cAMP standards, as described in the manufacturer's user manual. Data are analyzed by nonlinear regression analysis with the GraphPad Prism Software package (GraphPad Software, Inc., San Diego, Calif.) using the non-linear regression, one-site competition equation. The Cheng-Prusoff equation is used to calculate the K_(i), using the EC₅₀ of the oxotremorine concentration-response curve and the oxotremorine assay concentration as the K_(D) and [L], respectively. The K_(i) values are converted to pK_(i) values to determine the geometric mean and 95% confidence intervals. These summary statistics are then converted back to K_(i) values for data reporting.

In this assay, a lower K_(i) value indicates that the test compound has a higher functional activity at the receptor tested. The exemplified compounds of the invention are expected to have a K_(i) value of less than about 100 nM for blockade of oxotremorine-inhibition of forskolin-mediated cAMP accumulation in CHO-K1 cells expressing the hM₂ receptor. For example, the compound of Example 2 exhibited a K_(i) value of less than about 1.0 nM in this assay.

Blockade of Agonist-Mediated [³⁵S]GTPγS Binding

In a second functional assay, the functional potency of test compounds can be determined by measuring the ability of the compounds to block oxotremorine-stimulated [³⁵S]GTPγS binding in CHO-K1 cells expressing the hM₂ receptor.

At the time of use, frozen membranes are thawed and then diluted in assay buffer with a final target tissue concentration of 5-10 μg protein per well. The membranes are briefly homogenized using a Polytron PT-2100 tissue disrupter and then added to the assay plates.

The EC₉₀ value (effective concentration for 90% maximal response) for stimulation of [³⁵S]GTPγS binding by the agonist oxotremorine is determined in each experiment.

To determine the ability of a test compound to inhibit oxotremorine-stimulated [³⁵S]GTPγS binding, the following is added to each well of 96 well plates: 25 μL of assay buffer with [³⁵S]GTPγS (0.4 nM), 254 of oxotremorine (EC₉₀) and guanosine diphosphate (3 μM), 25 μL of diluted test compound and 25 μL CHO cell membranes expressing the hM₂ receptor. The assay plates are then incubated at 37° C. for 60 minutes. The assay plates are filtered over 1% BSA-pretreated GF/B filters using a PerkinElmer 96-well harvester. The plates are rinsed with ice-cold wash buffer for 3×3 seconds and then air or vacuum dried. Microscint-20 scintillation liquid (50 μL) is added to each well, and each plate is sealed and radioactivity counted on a topcounter (PerkinElmer). Data are analyzed by nonlinear regression analysis with the GraphPad Prism Software package (GraphPad Software, Inc., San Diego, Calif.) using the non-linear regression, one-site competition equation. The Cheng-Prusoff equation is used to calculate the K_(i), using the IC₅₀ values of the concentration-response curve for the test compound and the oxotremorine concentration in the assay as the K_(D) and [L], ligand concentration, respectively.

In this assay, a lower K_(i) value indicates that the test compound has a higher functional activity at the receptor tested. The exemplified compounds of the invention are expected to have a K_(i) value of less than about 100 nM for blockade of oxotremorine-stimulated [³⁵S]GTPγS binding in CHO-K1 cells expressing the hM₂ receptor.

Blockade of Agonist-Mediated Calcium Release Via FLIPR Assays

Muscarinic receptor subtypes (M₁, M₃ and M₅ receptors), which couple to G_(q) proteins, activate the phospholipase C (PLC) pathway upon agonist binding to the receptor. As a result, activated PLC hydrolyzes phosphatyl inositol diphosphate (PIP₂) to diacylglycerol (DAG) and phosphatidyl-1,4,5-diphosphate (IP₃), which in turn generates calcium release from intracellular stores, i.e., endoplasmic and sarcoplasmic reticulum. The FLIPR® (Molecular Devices, Inc.) assay capitalizes on this increase in intracellular calcium by using a calcium sensitive dye (Fluo-4AM, Molecular Probes) that fluoresces when free calcium binds. This fluorescence event is measured in real time by the FLIPR, which detects the change in fluorescence from a monolayer of cells cloned with hM₁, hM₃, and cM₅ receptors. Antagonist potency can be determined by the ability of antagonists to inhibit agonist-mediated increases in intracellular calcium.

For FLIPR calcium stimulation assays, CHO cells stably expressing the hM₁, hM₃ and cM₅ receptors are seeded into 96-well FLIPR plates the night before the assay is done. Seeded cells are washed twice by Cellwash (MTX Labsystems, Inc.) with FLIPR buffer (10 mM HEPES, pH 7.4, 2 mM calcium chloride, 2.5 mM probenecid in HESS without calcium and magnesium) to remove growth media and leaving 50 μL/well of FLIPR buffer. The cells are then incubated with 50 μL/well of 4 μM FLUO-4AM (a 2× solution was made) for 40 minutes at 37° C., 5% carbon dioxide. Following the dye incubation period, cells are washed two times with FLIPR buffer, leaving a final volume of 50 μL/well.

To determine antagonist potency, the dose-dependent stimulation of intracellular Ca²⁺ release for oxotremorine is first determined so that antagonist potency can later be measured against oxotremorine stimulation at an EC₉₀ concentration. Cells are first incubated with compound dilution buffer for 20 minutes, followed by agonist addition, which is performed by the FLIPR. An EC₉₀ value for oxotremorine is generated according to the method detailed in the FLIPR measurement and data reduction section below, in conjunction with the formula EC_(F)=((F/100−F)^1/H)*EC₅₀. An oxotremorine concentration of 3×EC_(F) is prepared in stimulation plates such that an EC₉₀ concentration of oxotremorine is added to each well in the antagonist inhibition assay plates.

The parameters used for the FLIPR are: exposure length of 0.4 seconds, laser strength of 0.5 watts, excitation wavelength of 488 nm, and emission wavelength of 550 nm. Baseline is determined by measuring the change in fluorescence for 10 seconds prior to addition of agonist. Following agonist stimulation, the FLIPR continuously measures the change of fluorescence every 0.5 to 1 second for 1.5 minutes to capture the maximum fluorescence change.

The change of fluorescence is expressed as maximum fluorescence minus baseline fluorescence for each well. The raw data is analyzed against the logarithm of drug concentration by nonlinear regression with GraphPad Prism (GraphPad Software, Inc., San Diego, Calif.) using the built-in model for sigmoidal dose-response. Antagonist K_(i) values are determined by Prism using the oxotremorine EC₅₀ value as the K_(D) and the oxotremorine EC₉₀ for the ligand concentration according to the Cheng-Prusoff equation (Cheng & Prusoff, 1973).

In this assay, a lower K_(i) value indicates that the test compound has a higher functional activity at the receptor tested. The exemplified compounds of the invention are expected to have a K_(i) value of less than about 100 nM for blockade of agonist-mediated calcium release in CHO cells stably expressing the hM₃ receptor.

Assay 3 Rat Einthoven Assay

This in vivo assay is used to assess the bronchoprotective effects of test compounds exhibiting muscarinic receptor antagonist activity.

All test compounds are diluted in sterile water and dosed via the inhalation route (IH). The rats (Sprague-Dawley, male, 250-350 g) are exposed to the aerosol generated from an LC Star Nebulizer Set and driven by a mixture of gases (5% CO₂/95% atmospheric air). Each test compound solution is nebulized over a 10 minute time period in a pie shaped dosing chamber capable of holding six animals. At predetermined time points after inhalation of compound, the Einthoven assay is performed.

Thirty minutes prior to the start of pulmonary evaluation, the animals are anesthetized with inactin (thiobutabarbital, 120 mg/kg IP). The jugular vein is catheterized with saline filled polyethylene catheters (PE-50) and used to infuse the bronchoconstrictor methylcholine (MCh). The trachea is then dissected and cannulated with a 14G needle and used for rat ventilation during pulmonary evaluation. Once surgery is complete, the animals are ventilated using a piston respirator set at a stroke volume of 1 ml/100 g body weight but not exceeding 2.5 ml volume, and at a rate of 90 strokes per minute.

The changes in pressure that occur with each breath are measured. Baseline values are collected for at least 2.5 minutes then the animals are challenged non-cumulatively with 2-fold incremental increases of MCh (5, 10, 20, 40 and 80 μg/ml). MCh is infused for 2.5 minutes from a syringe pump at a rate of 2 mL/kg/min. The animals are euthanized upon completion of the studies.

Changes in ventilation pressure (cm H₂O) in treated animals are expressed as % inhibition of MCh response relative to control animals. In this assay, a higher % inhibition value indicates that the test compound has a bronchoprotective effect. Exemplary compounds of the invention that are tested in this assay at a dose of 100 μg/ml are expected to exhibit greater than 35% inhibition, some are expected to exhibit greater than 70% inhibition, and some are expected to exhibit greater than 90% inhibition. For example, the compounds of Example 1 and Example 2 exhibited greater than 35% inhibition in this assay.

1.5 hr ID₅₀ Determination

Standard muscarinic antagonists were evaluated in the rat Einthoven assay 1.5 hours post-dose. The order of potency (ID₅₀s) for the five standards tested was determined to be: ipratropium (4.4 μg/ml)>tiotropium (6 μg/ml)>des-methyl-tiotropium (12 μg/ml)>glycopyrrolate (15 μg/ml)>LAS-34237 (24 μg/ml). The potency of the test compound is similarly determined at 1.5 hrs post-dose.

6 and 24 hr ID₅₀ Determination

Standards tiotropium and ipratropium were also evaluated 24 hours and/or 6 hours post-dose in the rat Einthoven assay. Ipratropium (10 and 30 μg/ml) was about 3-fold less potent 6-hours post-dose compared to its 1.5 hour potency. The observed loss of activity at this time point (6 hours) is consistent with its relatively short duration of action in the clinic. Tiotropium showed a slow onset of effect with peak bronchoprotection being achieved 6-hours post-dose. Its 6 hour and 24 hour potency values were not significantly different from each other and were about 2-fold more potent compared to its 1.5 hour potency. The onset of action of the test compound, as well as the 6 and 24 hour potency values, is similarly determined.

Assay 4 Rat Antisialagogue Assay

Rats (Sprague-Dawley, male, 250-350 g) are dosed, anesthetized and cannulated as described for Assay 3. At predetermined time points and after surgery, animals are placed on their dorsal side at a 20° incline with their head in a downward slope. A pre-weighed gauze pad is inserted in the animal's mouth and the muscarinic agonist pilocarpine (PILO) (3 mg/kg, IV) is administered. Saliva produced during 10 minutes post-PILO is measured gravimetrically by determining the weight of the gauze pad before and after PILO. Antisialagogue effects are expressed as % inhibition of salivation relative to control animals.

1, 6 and 24 hr ID₅₀ Determination

The rat antisialagogue assay was developed to assess systemic exposure and calculate the lung selectivity index (LSI) of test compounds. The standard, tiotropium, was evaluated in this model at 1, 6, and 24 hours post-dose. Tiotropium was found to be most potent at inhibiting pilocarpine-induced salivation 6 hours post dose. This finding is consistent with the peak effects observed in the Einthoven assay.

This model is a modified version of the procedure described in Rechter, “Estimation of anticholinergic drug effects in mice by antagonism against pilocarpine-induced salivation” Ata Pharmacol Toxicol 24:243-254 (1996). The mean weight of saliva in vehicle-treated animals, at each pre-treatment time, is calculated and used to compute % inhibition of salivation, at the corresponding pre-treatment time, at each dose.

Exemplary compounds of the invention that are tested in this assay are expected to exhibit ID₅₀ values less than 100 μg/ml (measured at 24 hours), with some compounds expected to exhibit an ID₅₀ value less than 30 μg/ml, some less than 20 μg/ml, and some less than 15 μg/ml.

The ratio of the anti-sialagogue ID₅₀ to bronchoprotective ID₅₀ is used to compute the apparent lung selectivity index of the test compound. Generally, compounds having an apparent lung selectivity index greater than about 5 are preferred.

While the present invention has been described with reference to specific aspects or embodiments thereof, it will be understood by those of ordinary skilled in the art that various changes can be made or equivalents can be substituted without departing from the true spirit and scope of the invention. Additionally, to the extent permitted by applicable patent statues and regulations, all publications, patents and patent applications cited herein are hereby incorporated by reference in their entirety to the same extent as if each document had been individually incorporated by reference herein. 

What is claimed is:
 1. A compound, having the formula IIb:

where: X⁻ is an anion of a pharmaceutically acceptable acid; R¹ is cyclopentyl; R³ is —OH; R⁵ is —C₁₋₅alkyl; R⁶ is —C₁₋₃alkyl; Z is a bond; Q is selected from thienyl, furanyl, pyrrolyl, pyrazolyl, benzo[1,3]dioxolyl, indolyl, and tetrazolyl; and pharmaceutically acceptable salts thereof.
 2. The compound of claim 1, wherein R⁵ is —CH₃; R⁶ is selected from —CH₃, —CH₂CH₃, and —(CH₂)₂CH₃; Q is selected from 1H-indol-3-yl, thiophen-2-yl, thiophen-3-yl, benzo[1,3]dioxol-5-yl, pyrrol-1-yl, and 1H-tetrazol-5-yl.
 3. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier.
 4. The composition of claim 3, wherein the compound is in micronized form.
 5. A method for treating a patient suffering from chronic obstructive pulmonary disease or asthma, comprising administering a therapeutically effective amount of the compound of claim
 1. 6. The method of claim 5, wherein the therapeutically effective amount is a bronchodilation-producing amount. 